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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
HCLUST
 
Resource Report
Resource Website
1000+ mentions
HCLUST (RRID:SCR_009154) HCLUST software application, software resource Software application that is a simple clustering method that can be used to rapidly identify a set of tag SNP's based upon genotype data (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, genetic, genomic, r, bio.tools is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
THIS RESOURCE IS NO LONGER IN SERVICE biotools:h-clust, SCR_009102, nlx_154195, nlx_154331 https://bio.tools/h-clust SCR_009154 R/HCLUST 2026-02-16 09:47:21 1459
Conrad Prebys Center for Chemical Genomics
 
Resource Report
Resource Website
Conrad Prebys Center for Chemical Genomics (RRID:SCR_001687) data or information resource, organization portal, portal The Conrad Prebys Center for Chemical Genomics (CPCCG) uses advanced screening technologies to identify high level chemical probes that interact with proteins involved in cellular processes. Optimization of these probes using medicinal chemistry and informatics will form the basis of a new generation of medicines. CPCCG is 1 of 4 Comprehensive Centers chosen nationally to be a part of the Molecular Libraries Probe Program (MLP), which established the Molecular Libraries Probe Production Centers Network (MLPCN). The goal is to produce small molecule probes that allow research into health and disease on the cellular level. CPCCG core services span a range of biochemical and cell-based screens for obtaining hits and provide chemistry resources for optimizing hits into probes or drug development. - Full scale screening capabilities and technology which can provide rapid screening on a broad diversity of assays and detection platforms - Several fully-integrated industrial-scale high-throughput screening (HTS) workstations - HTS microscopy/HCS and novel algorithm development for image analysis - Full hit-to-probe chemistry and exploratory pharmacology - Powerful NMR based Chemical Fragment Screening - Highly integrated informatics infrastructure and efficient data mining capabilities - Protein production facility - Cell production facility for scale-up tissue culture The CPCCG Screening Core can screen 96, 384 or 1536 well formats using either biochemical or cell-based assays, and can process over 300,000 wells per day. Total throughput capacity will climb to over 2 million compounds per day following the opening of Burnhams east coast campus in Lake Nona, Florida. drug, algorithm, analysis, assay, biochemical, cell, cellular, chemical, culture, development, disease, genomic, hcs, health, hts microscopy, keywords: chemical, medicinal, microscopy, molecular, molecule, probe, process, production, protein, technology, tissue, image Free, Freely Available nif-0000-10180 http://sdccg.burnham.org SCR_001687 CPCCG 2026-02-16 09:45:33 0
SoftBerry
 
Resource Report
Resource Website
100+ mentions
SoftBerry (RRID:SCR_000902) software resource, data or information resource, portal Developer of software tools for genomic research focused on computational methods of high throughput biomedical data analysis, including software to support next generation sequencing technologies, transcriptome analysis with RNASeq data, SNP detection and selection of disease specific SNP subsets. Provides custom genome annotation services. genomic, analysis, computation, biomedical, data analysis, rnaseq, sna, snp, transcriptome Restricted nlx_156881 http://linux1.softberry.com/ SCR_000902 Linux SoftBerry, Soft berry 2026-02-16 09:45:22 356
SOAP
 
Resource Report
Resource Website
100+ mentions
SOAP (RRID:SCR_000689) SOAP, data processing software, software application, software resource Software package that provides full solution to next generation sequencing data analysis consisting of an alignment tool (SOAPaligner/soap2), a re-sequencing consensus sequence builder (SOAPsnp), an indel finder ( SOAPindel ), a structural variation scanner ( SOAPsv ), a de novo short reads assembler ( SOAPdenovo ), and a GPU-accelerated alignment tool for aligning short reads with a reference sequence. (SOAP3/GPU)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, genetic, genomic, next generation sequencing, alignment, short read, bio.tools lists: SOAPfusion
lists: SOAPfuse
lists: SOAPnuke
lists: GapCloser
is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
has parent organization: BGI; Shenzhen; China
is parent organization of: SOAP3
is parent organization of: SOAPaligner/soap2
PMID:18227114 THIS RESOURCE IS NO LONGER IN SERVICE nlx_154652, biotools:soap https://bio.tools/soap SCR_000689 SOAP: short oligonucleotide alignment program, Short Oligonucleotide Analysis Package 2026-02-16 09:45:19 402
Blixem
 
Resource Report
Resource Website
1+ mentions
Blixem (RRID:SCR_015994) software application, data processing software, image analysis software, software resource, alignment software Software for sequence alignments that displays multiple match sequences aligned against a single genomic reference sequence. It can be used for manipulation, display and annotation of genomic data, to check the quality of an alignment, to find missing/misaligned sequence, and to identify splice sites and polyA sites. software, sequence, alignment, annotation, genomic, reference, data, display, manipulation, DNA is related to: SEQtools
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
Wellcome Trust Grant 098051;
NHGRI U54 HG00455
PMID:26801397 Free, Available for download SCR_015994 SEQtools Blixem 2026-02-16 09:48:55 2
IndelGenotyper
 
Resource Report
Resource Website
50+ mentions
IndelGenotyper (RRID:SCR_016663) GATK software application, data processing software, sequence analysis software, data analysis software, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 18th,2023. Software package for genome analysis. Used for analysis of next generation genomic data in cancer. next, generation, analysis, genomic, data, cancer, genome is listed by: Debian
has parent organization: Broad Institute
THIS RESOURCE IS NO LONGER IN SERVICE https://github.com/broadinstitute/gatk/
https://sources.debian.org/src/gatk/
SCR_016663 GATK Indel Genotyper, Genome Analysis Toolkit (GATK) Indel Genotyper, Indel Genotyper, GATK IndelGenotyper 2026-02-16 09:49:05 63
PiGx
 
Resource Report
Resource Website
1+ mentions
PiGx (RRID:SCR_016476) PiGx software application, data processing software, software toolkit, sequence analysis software, data analysis software, software resource Software application as a collection of genomic pipelines used for raw fastq read data of bisulfite experiments, RNAseq samples, single cell dropseq analysis, reads from ChIPseq experiments, analysis of sequence mutations in CRISPR-CAS9 targeted amplicon sequencing data. collection, genomic, pipeline, bisulfite, sequencing, rnaseq, chipseq, single, cell, reproducibility, sample, analysis, mutation, data German Federal Ministry of Education and Research (BMBF) 031 A538C RBC (de.NBI);
European Union Horizon 2020 No 654248
Free, Available for download, Freely available https://github.com/BIMSBbioinfo/pigx SCR_016476 Pipelines in Genomics 2026-02-16 09:49:02 6
Entrez
 
Resource Report
Resource Website
10+ mentions
Entrez (RRID:SCR_016640) web service, data access protocol, software resource, portal, data or information resource Web portal for global query cross database search and retrieval system that provides access to all databases simultaneously with a single query string and user interface. Retrieves nucleotide and protein sequence data, gene centered and genomic mapping information, 3D structures, and references. Covers databases including protein sequence data from PIR-International, PRF, Swiss-Prot, and PDB and nucleotide sequence data from GenBank that includes information from EMBL and DDBJ. global, query, cross, database, search, retrival, system, database, nucleotide, protein, sequence, data, genomic, mapping, structure, reference is affiliated with: PubChem BioAssay
is related to: National Library of Medicine
has parent organization: NCBI
works with: Batch Entrez
works with: Biotite
Free, Freely available SCR_016640 2026-02-16 09:49:04 15
DETONATE
 
Resource Report
Resource Website
1+ mentions
DETONATE (RRID:SCR_017035) DETONATE software application, data processing software, sequence analysis software, data analysis software, software resource Software tool to evaluate de novo transcriptome assemblies from RNA-Seq data. Consists of RSEM-EVAL and REF-EVAL packages. RSEM-EVAL is reference-free evaluation method. REF-EVAL is reference based and can be used to compare sets of any kinds of genomic sequences. evaluate, de novo, transcriptome, assembly, RNAseq, data, RSEM-EVAL, REF-EVAL, dataset, genomic, sequence, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: University of Wisconsin-Madison; Wisconsin; USA
NHGRI R01 HG005232;
NLM T15 LM007359
PMID:25608678 Free, Available for download, Freely available biotools:detonate https://bio.tools/detonate SCR_017035 DE novo TranscriptOme rNa-seq Assembly with or without the Truth Evaluation, DETONATE 2026-02-16 09:49:09 2
Diabetes Disease Portal
 
Resource Report
Resource Website
Diabetes Disease Portal (RRID:SCR_001660) Diabetes Disease Portal data set, topical portal, portal, data or information resource, disease-related portal An integrated resource for information on genes, QTLs and strains associated with diabetes. The portal provides easy acces to data related to both Type 1 and Type 2 Diabetes and Diabetes-related Obesity and Hypertension, as well as information on Diabetic Complications. View the results for all the included diabetes-related disease states or choose a disease category to get a pull-down list of diseases. A single click on a disease will provide a list of related genes, QTLs, and strains as well as a genome wide view of these via the GViewer tool. A link from GViewer to GBrowse shows the genes and QTLs within their genomic context. Additional pages for Phenotypes, Pathways and Biological Processes provide one-click access to data related to diabetes. Tools, Related Links and Rat Strain Models pages link to additional resources of interest to diabetes researchers. gene, quantitative trait locus, strain, diabetic complication, genome, gviewer, genomic, phenotype, pathway, biological process, chromosome, visualization, molecular function, cellular component, synteny is related to: NIDDK Information Network (dkNET)
is related to: Gene Ontology
has parent organization: Rat Genome Database (RGD)
Type 1 diabetes, Type 2 diabetes, Diabetes, Obesity, Hyperlipidemia, Metaboic disease, Hypertension Free, Freely Available nlx_153942 http://rgd.mcw.edu/rgdCuration/?module=portal&func=show&name=diabetes SCR_001660 2026-02-16 09:45:32 0
GATK
 
Resource Report
Resource Website
10000+ mentions
GATK (RRID:SCR_001876) GATK software application, data processing software, software toolkit, data analysis software, software library, software resource A software package to analyze next-generation resequencing data. The toolkit offers a wide variety of tools, with a primary focus on variant discovery and genotyping as well as strong emphasis on data quality assurance. Its robust architecture, powerful processing engine and high-performance computing features make it capable of taking on projects of any size. This software library makes writing efficient analysis tools using next-generation sequencing data very easy, and second it's a suite of tools for working with human medical resequencing projects such as 1000 Genomes and The Cancer Genome Atlas. These tools include things like a depth of coverage analyzers, a quality score recalibrator, a SNP/indel caller and a local realigner. (entry from Genetic Analysis Software) gene, genetic, genomic, next-generation resequencing, bio.tools is used by: Halvade Somatic
is listed by: OMICtools
is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
is related to: SnpEff
has parent organization: Broad Institute
PMID:21478889 Free, Available for download, Freely available nlx_154324, OMICS_00286, biotools:gatk http://www.broadinstitute.org/gsa/wiki/index.php/The_Genome_Analysis_Toolkit
https://bio.tools/gatk
SCR_001876 Genome Analysis ToolKit 2026-02-16 09:45:36 16663
MouseCyc
 
Resource Report
Resource Website
1+ mentions
MouseCyc (RRID:SCR_001791) MouseCyc data analysis service, analysis service resource, database, production service resource, service resource, data or information resource A manually curated database of both known and predicted metabolic pathways for the laboratory mouse. It has been integrated with genetic and genomic data for the laboratory mouse available from the Mouse Genome Informatics database and with pathway data from other organisms, including human. The database records for 1,060 genes in Mouse Genome Informatics (MGI) are linked directly to 294 pathways with 1,790 compounds and 1,122 enzymatic reactions in MouseCyc. (Aug. 2013) BLAST and other tools are available. The initial focus for the development of MouseCyc is on metabolism and includes such cell level processes as biosynthesis, degradation, energy production, and detoxification. MouseCyc differs from existing pathway databases and software tools because of the extent to which the pathway information in MouseCyc is integrated with the wealth of biological knowledge for the laboratory mouse that is available from the Mouse Genome Informatics (MGI) database. energy production, biosynthesis, cell, cellular, degradation, detoxification, metabolism, mouse, physiological, enzymatic reaction, gene, disease, genome, metabolic pathway, pathway, compound, enzymatic reaction, protein, rna, reaction, blast, human, mammal, genetic, genomic is related to: Mouse Genome Informatics (MGI)
is related to: Gene Ontology
has parent organization: Jackson Laboratory
NHGRI HG003622 PMID:19682380 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-10303 SCR_001791 MouseCyc database, Mouse Genome Informatics: MouseCyc database 2026-02-16 09:45:35 9
Rice Genome Research Project
 
Resource Report
Resource Website
1+ mentions
Rice Genome Research Project (RRID:SCR_002268) database, data or information resource, topical portal, portal Rice Genome Research Program (RGP) is an integral part of the Japanese Ministry of Agriculture, Forestry and Fisheries (MAFF) Genome Research Project. RGP now aims to completely sequence the entire rice genome and subsequently to pursue integrated goals in functional genomics, genome informatics and applied genomics. It is jointly coordinated by the National Institute of Agrobiological Sciences (NIAS), a government research institute under MAFF and the Society for Techno-innovation of Agriculture, Forestry and Fisheries (STAFF), a semi-private research organization managed and supported by MAFF and a consortium of some twenty Japanese companies. The research is funded with yearly grants from MAFF and additional funds from the Japan Racing Association (JRA). It is now the leading member of the International Rice Genome Sequencing Project (IRGSP), a consortium of ten countries sharing the sequencing of the 12 rice chromosomes. The IRGSP adopts the clone-by-clone shotgun sequencing strategy so that each sequenced clone can be associated with a specific position on the genetic map and adheres to the policy of immediate release of the sequence data to the public domain. In December 2004, the IRGSP completed the sequencing of the rice genome. The high-quality and map-based sequence of the entire genome is now available in public databases. fishery, forestry, functional, genetic, agriculture, chromosome, clone, genome, genomic, informatic, map, rice, sequence, sequencing, shotgun PMID:9482829 Free, Freely available nif-0000-20992 SCR_002268 Rice Genome Research Project 2026-02-16 09:45:43 4
Yeast consensus metabolic network - A consensus reconstruction of yeast metabolism
 
Resource Report
Resource Website
1+ mentions
Yeast consensus metabolic network - A consensus reconstruction of yeast metabolism (RRID:SCR_002135) database, data or information resource, topical portal, portal This is a portal to the consensus yeast metabolic network as reconstructed from the genome sequence and literature. It is a highly annotated metabolic map that is periodically updated by a team of collaborators from various research groups. The first version of this reconstruction was published in Herrgrd, Swainston et al. (2008) A consensus yeast metabolic reconstruction obtained from a community approach to systems biology Nature Biotechnol. 26, 1155-1160 (you can access that network here). A second version has now been released and is awaiting publication. We plan on continuing to update this resource towards a complete metabolic network of yeast. All versions will remain accessible for historical purposes, however it is highly recommended that you always use the latest one since that is the most up to date. This effort started on the shoulders of a number of reconstructions of the metabolic network of yeast based on genomic and literature data that were published separately. (iMM904 and iLL672) However, due to the different approaches utilized in them, those earlier reconstructions had a significant number of differences. In addition they suffered from the use of non-standard names and overall they were not annotated with methods that are machine-readable. A community effort in 2007, led by the Manchester Centre for Integrative Systems Biology and the YSBN resulted in a consensus network representation of yeast metabolism, reconciling the earlier results. That effort is now ongoing under the leadership of the MCISB and with collaboration with colleagues under the UNICELLSYS FP7 project. Availability The network reconstruction is primarily assembled and provided as an SBML file enriched with MIRIAM-compliant annotations (which are embedded in the SBML through RDF). All small and macro- molecules are referenced to an authoritative database (e.g. Uniprot, ChEBI, etc.). All molecules and reactions are also annotated with appropriate publications that contain supporting evidence. Thus this network is entirely traceable and is presented in a computational framework. SBML is a format that is understood by a large number of software applications (see sbml.org). While the SBML file is the most efficient computational resource for these data, casual users also need access to the network. That is provided by a searchable relational database accessed directly from this website. The database pages also allow readers to add comments to any chemical species or reaction. Such comments are taken into consideration by the team collating new versions of the network and can lead to corrections and additions to the network. This reconstruction is provided in the following formats: :* an SBML file containing the reaction network and annotations, located to specific sub-cellular compartments :* an SBML file containing the reaction network and annotations without subcellular compartmentation (all reactions happening in a single compartment). :* a searcheable relational database, which uses the B-Net software from Pedro Mendes' group. The database version of this data set is managed with the B-Net software created in Pedro Mendes' group at the Virginia Bioinformatics Institute. B-Net's schema is a detailed representation of the underlying biochemistry and regulation. A number of reconstructions of the metabolic network of yeast based on genomic and literature data have been published. However, due to different approaches utilized in the reconstruction as well as different interpretations of the literature, the earlier reconstructions have significant number of differences. A community effort resulted in a consensus network model of yeast metabolism, combining results from previous models. genomic, literature, metabolic network, yeast Free, Freely available nif-0000-20926 SCR_002135 Yeast consensus metabolic network 2026-02-16 09:45:41 8
OMICtools
 
Resource Report
Resource Website
10+ mentions
OMICtools (RRID:SCR_002250) OMICtools data or information resource, database, catalog THIS RESOURCE IS NO LONGER IN SERVICE. Documented Jul 19, 2024. Metadatabase manually curated that provides web accessible tools related to genomics, transcriptomics, proteomics and metabolomics. Used as informative directory for multi-omic data analysis. metadatabase, manually, curated, tool, genomic, transcriptomic, proteomic, metabolomic, data lists: ncdfFlow
lists: BSmooth-align
lists: 4Peaks
lists: CSDeconv
lists: Tablet
lists: GenomicRanges
lists: SNPSVM
lists: ReadqPCR
lists: SP-Designer
lists: CorMut
lists: ChIPmeta
lists: FACS
lists: metaSeq
lists: Dissect
lists: Fusion Analyser
lists: FusionCatcher
lists: GASV
lists: GHOSTM
lists: nFuse
lists: PD5
lists: Patchwork
lists: QuadGT
lists: VariantAnnotation
lists: ReQON
lists: SnowsShoes-FTD
lists: timecourse
lists: SOAPfuse
lists: SOAPfusion
lists: pFind Studio: pLink
lists: Spotfinder
lists: AbMining ToolBox
lists: SNAVI
lists: MetAssign
lists: JChemPaint
lists: siRNArules
lists: AutoPrime
lists: RmiR.Hs.miRNA
lists: MysiRNA-designer
lists: TACOA
lists: Treephyler
lists: MedGen
lists: D-Tailor
lists: BioLemmatizer
lists: AffyRNADegradation
lists: Orphelia
lists: ArrayExpress (R)
lists: Parallel-META
lists: CovalentDock Cloud
lists: DOCK
lists: exomeSuite
lists: SPAdes
lists: Sequence Read Format
lists: FastQ Screen
lists: GEOquery
lists: Bovine Genome Database
lists: GISTIC
lists: DESeq
lists: Postgwas
lists: BLASTPLOT
lists: miRanalyzer
lists: Magnolya
lists: GMATo
lists: GemSIM
lists: Grinder
lists: Illuminate
lists: RNAcontext
lists: MIMOSA
lists: F2DockClient
lists: FlexX
lists: Glide
lists: GOLD
lists: Molegro Virtual Docker
lists: Sanjeevini
lists: SODOCK
lists: HEM
lists: Surflex-Dock
lists: Cascleave
lists: MetaDE
lists: Cell Death Proteomics Database
lists: GPS-Calpain Cleavage Detector
lists: GraBCas
lists: c3net
lists: Context Likelihood of Relatedness
lists: GENIE3
lists: Inferelator
lists: MODENT - A Tool For Reconstructing Gene Regulatory Networks
lists: MRNet
lists: UnSplicer
lists: Duplicate reads removal
lists: PEpiD
lists: TAPIR: target prediction for plant microRNAs
lists: iOMICS
lists: Megraft
lists: VARiD
lists: Cistrome
lists: PSGInfer
lists: MochiView
lists: RSEM
lists: RNAmotifs
lists: M(at)CBETH
lists: MS-Spectre
lists: Quant
lists: RNASeqReadSimulator
lists: iFad
lists: GramCluster
lists: GProX
lists: PeptideProphet
lists: CNTools
lists: Lasergene's SeqMan Pro
lists: ProteinProphet
lists: OMSSAPercolator
lists: Flicker
lists: cn.FARMS
lists: LIPAGE
lists: DNASTAR: Lasergene Core Suite
lists: Clonality
lists: oneClickCGH
lists: CGH Fusion
lists: Screensaver
lists: fqzcomp
lists: ArrayPlex
lists: MiRdup
lists: MeQA
lists: Methyl-Analyzer
lists: Annotare
lists: CpGassoc
lists: Koadarray
lists: RADtools
lists: rtd
lists: ABrowse
lists: GPViz
lists: cuteNMR
lists: Jnomics
lists: JMolDraw
lists: CGAP-Align
lists: ARACHNE
lists: Kinannote
lists: CLC Main Workbench
lists: ParseCNV
lists: TAPS
lists: PyroHMMsnp
lists: TransView
lists: pvac
lists: riboPicker
lists: NucleoFinder
lists: bzip2
lists: GENSENG
lists: AS-Peak
lists: is-rSNP
lists: ILLUMINUS
lists: QUALIFIER
lists: FunctSNP
lists: Micro-Analyzer
lists: flowStats
lists: flowPeaks
lists: metaMA
lists: rTANDEM
lists: flowFlowJo
lists: TargetCaller
lists: PSCBS
lists: iASeq
lists: d2-tools
lists: PEPPER
lists: OLINgui
lists: TNO-DECO
lists: SigFuge
lists: stsPlots
lists: Sulfinator
lists: Rdisop
lists: pbcore
lists: GeneExpressionSignature
lists: sybil - Efficient Constrained Based Modelling in R
lists: msbwt
lists: MetaDrug
lists: Reprever
lists: POPBAM
lists: SAMBLASTER
lists: SpeedSeq
lists: pyQPCR
lists: RefFinder
lists: PGS
lists: miRprimer
lists: iBMQ
lists: NIMBL
lists: TDARACNE
lists: bamova
lists: BAIT
lists: ARNIE
lists: fourSig
lists: Mfuzz
lists: MaryGold
lists: TOPPAS
lists: SPHINX
lists: PhyloPythia
lists: MATCHCLIP
lists: mzMatch
lists: Sequence Search and Alignment by Hashing Algorithm
lists: ESPRIT
lists: DySC
lists: FPSAC
lists: Scaffold builder
lists: SNPiR
lists: ACCUSA2
lists: MuTect
lists: Pindel
lists: rSeq
lists: GERP
lists: SiPhy
lists: wANNOVAR
lists: ViReMa
lists: Smart Dictionary Lookup
lists: VariantMaster
lists: GeneWays
lists: AdaptiveCrawler
lists: NGS-Cleaner
lists: flowQ
lists: Database Enabled Code for Ideal Probe Hybridization Employing R
lists: NGSmethPipe
lists: Pyrocleaner
lists: DecGPU
lists: drFAST
lists: MPscan
lists: TAPyR
lists: MutPred Splice
lists: ContEst
lists: Mini Analysis Guide for Microarrays
lists: DDBJ Omics Archive
lists: Chromas
lists: OnEx - Ontology Evolution Explorer
lists: BEBaC
lists: FlipFlop
lists: Phosphor Antibody Array Data Analysis
lists: PhenoFam
lists: forqs
lists: GMcloser
lists: GenomeWeb
lists: Bycom
lists: CorQ
lists: NGS tools for the novice
lists: Opera
lists: SRMA
lists: DeNovoGear
lists: VarB
lists: BAMseek
lists: TriageTools
lists: clipcrop
lists: detecttd
lists: FastUniq
lists: GEUVADIS
lists: TMAP
lists: BISMA
lists: FineSplice
lists: RMAP
lists: Sequencing Analysis Software
lists: BLASR
lists: GlycoWorkbench
lists: jmzIdentML API
lists: SciRoKo
lists: HapCompass
lists: JBrowse
lists: DSRC
lists: fastqz
lists: GDC
lists: GRS
lists: PREFAB
lists: BLASTP
lists: Google Compute Engine
lists: SplitSeek
lists: ASC
lists: NPEBseq
lists: FUSIM
lists: Geoffs Bio-Directories
lists: Phred
lists: MassGenomics
lists: Illuminator
lists: BAC
lists: targetscan.Hs.eg.db
lists: RmiR
lists: MmPalateMiRNA
lists: Starr
lists: bsseq
lists: Qvalue
lists: ExomePeak
lists: NextGenSeq(at)nature.com
lists: AutoAssemblyD
lists: CUDA-EC
lists: rGADEM
lists: qips
lists: PICS
lists: Jmosaics
lists: SparseAssembler
lists: BreakFusion
lists: ParticleCall
lists: DSGseq
lists: R453Plus1Toolbox
lists: SynView
lists: ShortFuse
lists: Cancer Gene Index
lists: jmzML
lists: CASVM
lists: Birdseed
lists: Reaper - Demultiplexing trimming and filtering sequencing data
lists: GimmeMotifs
lists: skewer
lists: flowWorkspace
lists: massiR
lists: Transposon Insertion Finder
lists: Shimmer
lists: GenVision
lists: DiMO
lists: MetaPhyl
lists: WiggleTools
lists: EMI
lists: SplicePlot
lists: CrossMap
lists: GraphIBD
lists: rbsurv
lists: Skylign
lists: HMMvar
lists: tbvar
lists: STRViper
lists: Breakway
lists: Genometa
lists: CATCHprofiles
lists: VAAL
lists: SLOPE
lists: BreakSeq
lists: Anchored Assembly
lists: Bionimbus
lists: ChIPMunk
lists: RDPipeline
lists: PeakAnalyzer
lists: SomaticCall
lists: Baa.pl
lists: VirusHunter
lists: seq2HLA
lists: MUMmerGPU
lists: GeneMeta
lists: GenoMiner
lists: GenoViewer
lists: sim4cc
lists: GenomicTools
lists: Omixon Target HLA Typing
lists: Omixon Target Data Analysis
lists: PARalyzer
lists: QualiMap
lists: Lab7
lists: mlgt
lists: BSSim
lists: Golden Helix GenomeBrowse
lists: HiPipe
lists: MADAM
lists: Microarray Data Analysis System
lists: Automated Microarray Pipeline
lists: MergeMaid
lists: OmicsOffice for NGS SeqSolve
lists: categoryCompare
lists: metahdep
lists: Plantagora
lists: QUAST
lists: TileQC
lists: VectorFriends
lists: vcflib
lists: PHACCS
lists: Sequedex
lists: Genome Trax
lists: VCFtools
lists: NGSUtils
lists: ChIP-seq
lists: Tally
lists: mapDamage
lists: freeIbis
lists: piCALL
lists: ERGO
lists: TALLYMER
lists: KMC
lists: DSK
lists: Mutation Surveyor
lists: BFCounter
lists: snpStats: SnpMatrix and XSnpMatrix classes and methods
lists: CNVtools
lists: CGEN
lists: RCASPAR
lists: iterativeBMAsurv
lists: multtest
lists: globaltest
lists: SABER
lists: Local Ancestry in adMixed Populations
lists: GemTools
lists: MinimumDistance
lists: ipPCA
lists: ADMIXTURE
lists: frappe
lists: Mutascope
lists: metabnorm
lists: VegaMC
lists: VanillaICE
lists: SNPchip
lists: SMAP
lists: quantsmooth
lists: mBPCR
lists: ITALICS
lists: GenoSet
lists: exomeCopy
lists: CGHregions
lists: CGHbase
lists: BlindCall
lists: beadarraySNP
lists: SSCprofiler
lists: CGH-Explorer
lists: GLAD
lists: SNP and Variation Suite SNP Analysis
lists: SNP and Variation Suite CNV Analysis
lists: ProbRNA
lists: methylMnM
lists: methyAnalysis
lists: les
lists: ARRmNormalization
lists: ChIPsim
lists: Sherman
lists: yaqcaffy
lists: wateRmelon
lists: sRAP
lists: spotSegmentation
lists: SNM
lists: SNAGEE
lists: Simpleaffy
lists: qcmetrics
lists: OLIN
lists: MANOR
lists: limmaGUI
lists: ffpe
lists: dyebias
lists: DEXUS
lists: BeadDataPackR
lists: aroma.light
lists: ArrayTools
lists: beadarray
lists: arrayQuality
lists: arrayMvout
lists: affyQCReport
lists: affyPLM
lists: affylmGUI
lists: AffyExpress
lists: waveTiling
lists: KAnalyze
lists: gprege
lists: oneChannelGUI
lists: CYCLE
lists: LMGene
lists: factDesign
lists: pickgene
lists: betr
lists: NGSrich
lists: SCAN.UPC
lists: arrayQualityMetrics
lists: CALIB
lists: DEDS
lists: Harshlight
lists: MiChip
lists: OCplus
lists: bridge
lists: FARMS
lists: fRMA
lists: genArise
lists: lapmix
lists: maCorrPlot
lists: maSigPro
lists: MACAT
lists: maigesPack
lists: MDQC
lists: metaArray
lists: nnNorm
lists: plgem
lists: PVCA
lists: RAMA
lists: stepNorm
lists: virtualArray
lists: LPE
lists: DDBJ Sequence Read Archive
lists: WegoLoc
lists: Mugsy
lists: Mspire-Simulator
lists: CytoSPADE
lists: vsn
lists: ACME
lists: GenGIS
lists: CoGAPS
lists: NTAP
lists: ToppCluster
lists: PyLOH
lists: Nebula
lists: Sequencher
lists: flowFP
lists: ChIPseeqer
lists: CisGenome
lists: CGHcall
lists: rMAT
lists: TileMap
lists: Clustal Omega
lists: BLASTN
lists: SeqScape Software
lists: BACContigEditor
lists: Human Gene Mutation Database
lists: AnimalTFDB
lists: asSeq
lists: Cuffdiff
lists: BLASTX
lists: SLqPCR
lists: rSeqDiff
lists: AffinDB
lists: Enriched Domain Detector
lists: A Classification of Mobile genetic Elements
lists: PELICAN
lists: nondetects
lists: rlsim
lists: Chilibot: Gene and Protein relationships from MEDLINE
lists: unifiedWMWqPCR
lists: HAPLOPAINTER
lists: HOMOZYGOSITYMAPPER
lists: QuasiSeq
lists: sSeq
lists: GERMLINE
lists: MCMC.qpcr
lists: CNVrd2
lists: TaLasso
lists: pairedBayes
lists: RNASeqBias
lists: plateCore
lists: PLINK
lists: MACH 1.0
lists: PennSeq
lists: FACTA+.
lists: Prediction of Amyloid Structure Aggregation
lists: TANGO
lists: DNACLUST
lists: InterMine
lists: MSClust
lists: ReCount - A multi-experiment resource of analysis-ready RNA-seq gene count datasets
lists: RSVSim
lists: TCC
lists: SAMstrt
lists: pRESTO
lists: MEME Suite - Motif-based sequence analysis tools
lists: PoissonSeq
lists: CQN
lists: GLiMMPS
lists: TEMP
lists: BEAGLE
lists: SPP
lists: BIRDSUITE
lists: NASTIseq
lists: BREAKDANCER
lists: CAROL
lists: COMPASS
lists: CASAVA
lists: flowClust
lists: HSA
lists: SPADE
lists: AStalavista
lists: Visual Molecular Dynamics
lists: EXTREME
lists: CYRILLIC
lists: DINDEL
lists: ASprofile
lists: OrderedList
lists: GenABEL
lists: CCAT
lists: Alt Event Finder
lists: BroadPeak
lists: SamSPECTRAL
lists: THetA
lists: TCW
lists: GATK
lists: Degust
lists: flowUtils
lists: DAVID
lists: RchyOptimyx
lists: StatAlign
lists: Arabidopsis thaliana Protein Interactome Database
lists: FGED
lists: ExpressionPlot
lists: S-MART
lists: Pecan
lists: SeqMonk
lists: Ray
lists: tbrowse
lists: Bacteriome.org
lists: Apollo
lists: RAVEN
lists: PEDIGRAPH
lists: BAliBASE
lists: TEQC
lists: rSNPs MAPPER
lists: rSNPBase
lists: SNP Function Portal
lists: flowType
lists: SNPper
lists: MADELINE
lists: CanSNPer
lists: ADaCGH2
lists: SGA
lists: NormaCurve
lists: GapMis
lists: TRAMS
lists: SNPMeta
lists: SNPAAMapper
lists: METAL
lists: OLORIN
lists: openADAM
lists: SeqEM
lists: SHARCGS
lists: DMET-Analyzer
lists: PEDHUNTER
lists: AffyPipe
lists: pSTIING
lists: PTMcode
lists: SHORTY
lists: POLYMUTT
lists: TissueNet - The Database of Human Tissue Protein-Protein Interactions
lists: TRIP Database
lists: SNVer
lists: BISC
lists: Primate Orthologous Exon Database
lists: PurBayes
lists: PyroHMMvar
lists: flowViz
lists: ChIPSeq Peak Finder
lists: SpliceAid-F
lists: Vennt
lists: flowTrans
lists: Spliceosome Database
lists: cisRED: cis-regulatory element
lists: ASPicDB
lists: SAMTOOLS
lists: HEXEvent
lists: DBASS
lists: FlyFactorSurvey
lists: SNAP - SNP Annotation and Proxy Search
lists: STIFDB
lists: Cake
lists: MPromDb
lists: ProTISA
lists: circlize
lists: AmiGO
lists: flowQB
lists: Cinteny
lists: RegPrecise
lists: STRUCTURE
lists: SVA
lists: SYZYGY
lists: TcoF
lists: Matchprot
lists: WebGeSTer DB
lists: pfSNP
lists: shinyTANDEM
lists: CistromeMap
lists: metaRNASeq
lists: ZOOM
lists: flowPlots
lists: ImaGene
lists: VAAST
lists: ARACNE
lists: FR-HIT
lists: PROVEAN
lists: flowPhyto
lists: flowCore
lists: flowMerge
lists: RankAggreg
lists: ConsensusPathDB
lists: MAIA (Microarray Image Analysis)
lists: CORUM
lists: CoryneRegNet
lists: miso-lims
lists: COSMIC - Catalogue Of Somatic Mutations In Cancer
lists: cpnDB: A Chaperonin Database
lists: flowMap
lists: rmeta
lists: flowMeans
lists: CTCFBSDB
lists: spliceR
lists: flowMatch
lists: flowFit
lists: DEMI
lists: Binding MOAD
lists: DBD: Transcription factor prediction database
lists: CodonCodes TraceViewer
lists: RelocaTE
lists: MAGE
lists: flowCyBar
lists: Iterative Signature Algorithm
lists: Variant Reporter Software
lists: RepARK
lists: PolyPhred
lists: dbSNP
lists: BEETL-fastq
lists: DWGSIM
lists: Ensembl
lists: DBTBS
lists: MIAME
lists: MAQC
lists: HaploClique
lists: DBTSS: Database of Transcriptional Start Sites
lists: DNA DataBank of Japan (DDBJ)
lists: ISO
lists: SBARS
lists: Clinical and Laboratory Standards Institute
lists: JGI Genome Portal
lists: Cancer Genomics Consortium
lists: BEAT
lists: DOMINO: Domain peptide interactions
lists: R Tutorial - An R Introduction to Statistics
lists: R Tutorial
lists: DOMINE: Database of Protein Interactions
lists: GenomeSmasher
lists: DOSY Toolbox
lists: MUMA
lists: Database of Rice Transcription Factors
lists: VennDiagram
lists: Quick-R
lists: EcoCyc
lists: Tree of Life
lists: flowBeads
lists: EDAS - EST-Derived Alternative Splicing Database
lists: eggNOG
lists: NRDR
lists: YLoc
lists: CAMERA - Collection of annotation related methods for mass spectrometry data
lists: EID: Exon-Intron Database
lists: WoLF PSORT
lists: Entrez Gene
lists: Mason
lists: QualitySNPng
lists: EPDnew
lists: realSFS
lists: pymzML
lists: RUbioSeq
lists: PBSIM
lists: PennCNV
lists: pIRS
lists: PeptideShaker
lists: ShotGun
lists: Gibbs Motif Sampler
lists: Zebrafish Information Network (ZFIN)
lists: Wessim
lists: BioStar
lists: MBASED
lists: discoSnp
lists: RVD
lists: SEEK
lists: MethylAid
lists: ExomeDepth
lists: libmgf
lists: Autophagy Database
lists: T3DB
lists: RopeBWT2
lists: e-Driver
lists: sapFinder
lists: PharmGKB
lists: CTF
lists: SuperTarget
lists: DrugBank
lists: PANDAseq
lists: NCBI database of Genotypes and Phenotypes (dbGap)
lists: leeHom
lists: Reflect
lists: Mapix
lists: Rainbow
lists: CASBAH
lists: TelSeq
lists: Pathview
lists: GLProbs
lists: rBiopaxParser
lists: DSS
lists: GATE
lists: NetPathMiner
lists: NMR metabolomics database of Linkoping
lists: GenBank
lists: HINT
lists: libCSAM
lists: RNA Abundance Database
lists: GeneCards
lists: BINOCh
lists: AliView
lists: TherMos
lists: ANDES
lists: PacmonSTR
lists: RMassBank
lists: FisHiCal
lists: Mutation Annotation and Genomic Interpretation
lists: Circleator
lists: IMEx - The International Molecular Exchange Consortium
lists: Batch Oligo Selection Script
lists: iontree
lists: MicroVigene
lists: Greengenes
lists: Basic4Cseq
lists: rDock
lists: hot scan
lists: International HapMap Project
lists: BiGGR
lists: mzR
lists: PAPi
lists: pNovo+
lists: COV2HTML
lists: CODEHOP
lists: CNVassoc
lists: PRO
lists: Hollywood
lists: StreamingTrim
lists: pLabel
lists: HomoloGene
lists: aCGH.Spline
lists: pBuild
lists: Time-series RNA-seq Analysis Package
lists: CGHnormaliter
lists: Type-III-Secretion-System related database
lists: SMRT-Analysis
lists: CPTRA
lists: mtDB - Human Mitochondrial Genome Database
lists: AltAnalyze - Alternative Splicing Analysis Tool
lists: Chimera
lists: IMG System
lists: Babelomics
lists: MRFSEQ
lists: ms lims
lists: ChIPMonk
lists: Gel2DE
lists: UCSF Spot
lists: ProRata
lists: R-pbutils
lists: MITOMAP - A human mitochondrial genome database
lists: NOISeq
lists: Dpos
lists: Gene Weaver
lists: pFind
lists: Canadian College of Medical Geneticists
lists: BRAIN
lists: Isopat
lists: R-pbh5
lists: pbh5tools
lists: SMRT View
lists: JASPAR
lists: enviPat
lists: bwtool
lists: MoSDi
lists: tweeDEseq
lists: DIALIGN
lists: PacBioToCA
lists: DiNuP
lists: Gutentag
lists: Parametric Time Warping
lists: SurvComp
lists: SASqPCR
lists: enviPick
lists: GeneFisher
lists: Triplex
lists: MPprimer
lists: MIPE
lists: MFEprimer
lists: DnaSP
lists: FAS-DPD
lists: SURPI
lists: MAPPER - Multi-genome Analysis of Positions and Patterns of Elements of Regulation
lists: MachiBase
lists: Primer3Plus
lists: e-PCR
lists: NeuroMab
lists: In-Silico PCR
lists: JETTA
lists: MapViewer
lists: Primer-BLAST
lists: WormBase
lists: eQtlBma
lists: JuncBASE
lists: MethDB
lists: pairheatmap
lists: MISO
lists: HYDEN
lists: mrsFAST
lists: PredictNLS
lists: mrCaNaVaR
lists: NovelSeq
lists: PlantLoc
lists: Primer3
lists: FastSNP
lists: Proteome Analyst Specialized Subcellular Localization Server
lists: NYCE
lists: GeneScissors
lists: ngLOC
lists: MultiLoc
lists: GeneCruiser
lists: MetaLocGramN
lists: FastPCR
lists: miRNAMap
lists: HUPO Proteomics Standards Initiative
lists: SaskPrimerFS
lists: rDiff
lists: Database of Interacting Proteins (DIP)
lists: Solas
lists: Pipeliner
lists: iLoc-Animal
lists: QDNAseq
lists: ResponseNet
lists: SynSysNet
lists: XORRO
lists: Stacks
lists: SECISearch3 and Seblastian
lists: SALT
lists: HyperTree
lists: Primer Designer
lists: r3Cseq
lists: Gene Set Enrichment Analysis
lists: Piano
lists: PHAST
lists: NHGRI: Establishing a Central Resource of Data from Genome Sequencing Projects
lists: NGSadmix
lists: Gemi
lists: Talking Glossary of Genetic Terms
lists: PathGuide: the pathway resource list
lists: SplicingCompass
lists: RNAhybrid
lists: LUMPY
lists: Geospiza
lists: SpliCQ
lists: ORFprimer
lists: JCVI Primer Designer
lists: Assembly Based ReAligner
lists: deFuse
lists: Xenbase
lists: PoPoolation2
lists: OmicCircos
lists: Amplicon
lists: PrimerSeq
lists: Genedata Expressionist
lists: biobambam
lists: RCircos
lists: ggbio
lists: DAFGA
lists: MIPgen
lists: PicTar
lists: BlockClust
lists: PIRSF
lists: miR-PREFeR
lists: MouseNET
lists: PlantProm DB
lists: MAGI
lists: PLANTTFDB
lists: ALDEx2
lists: qBasePLUS
lists: RefGenes
lists: HTqPCR
lists: BestKeeper
lists: NanoStringNorm
lists: NormFinder
lists: NormqPCR
lists: PolymiRTS
lists: PPDB: Plant Promoter Database
lists: ddCt
lists: GEOSS
lists: PReMod
lists: EasyqpcR
lists: NanoStriDE
lists: GBSA
lists: LaSSO
lists: NAPPA
lists: nSolver Analysis Software
lists: MAGENTA
lists: MetABEL
lists: ProNIT
lists: genomation
lists: metagen
lists: BMIQ
lists: FadE
lists: metaphor
lists: SWAN
lists: PROSITE
lists: Parseq
lists: qPrimerDepot
lists: Bpipe
lists: Nestly
lists: Snakemake
lists: SNAPE-pooled
lists: NGSANE
lists: jmzTab
lists: JISTIC
lists: Savant
lists: MetaSKAT
lists: Human Variome Project
lists: PoPoolation
lists: RefSeq
lists: MultiPhen
lists: RegulonDB
lists: MF-GE
lists: PheWAS R Package
lists: EBSeq
lists: MSMS
lists: RAREMETAL
lists: RevMan
lists: GEPAT
lists: Polyester
lists: SET
lists: J-Express
lists: UEA sRNA toolkit
lists: Osprey
lists: RINS
lists: PyroBayes
lists: PEAR
lists: JATAC
lists: SeqExpress
lists: Quantitative Enrichment of Sequence Tags
lists: Pash 3.0
lists: Factorbook
lists: FlyTF.org
lists: My Cancer Genome
lists: Pathosystems Resource Integration Center
lists: MSG
lists: InsertionMapper
lists: PubMed Central
lists: GeneCommittee
lists: INMEX
lists: TagDust
lists: PASS-bis
lists: HLASeq
lists: FIDEA
lists: EGAPP
lists: DCTD
lists: Hapmix
lists: BamView
lists: PerM
lists: Mercury
lists: CDP
lists: CB-Commander
lists: BSRD
lists: DER Finder
lists: Artemis: Genome Browser and Annotation Tool
lists: PeaKDEck
lists: PubChem
lists: Babel
lists: bcbio-nextgen
lists: SIDER
lists: EpiGRAPH
lists: DRUT
lists: Ancestrymap
lists: VIROME
lists: Vanator
lists: FACIL
lists: Velvet-SC
lists: SNiPer-HD
lists: Squeezambler
lists: UniGene
lists: SCPD - Saccharomyces cerevisiae promoter database
lists: GASSST
lists: SnoopCGH
lists: Taverna
lists: PASHA
lists: miRDeepFinder
lists: STAR
lists: Spanki
lists: VAMPS
lists: Basic OligoNucleotide Design
lists: Tree and reticulogram REConstruction
lists: ACT: Artemis Comparison Tool
lists: SPInDel
lists: Kdetrees
lists: tree editor
lists: Genomedata
lists: BioDiscovery Nexus Copy Number
lists: TETRA
lists: MetaCluster-TA
lists: DELLY
lists: QuickGO
lists: TAIR
lists: CompostBin
lists: Nonpareil
lists: BioPig
lists: LMAT
lists: AbundanceBin
lists: TaxSOM
lists: NuChart
lists: ProViDE
lists: UnifiedGenotyper
lists: SOrt-ITEMS
lists: RAIphy
lists: Human DNA Polymerase Gamma Mutation Database
lists: Pfam
lists: Distributed String Mining Framework
lists: Pplacer
lists: deStruct
lists: Phymm and PhymmBL
lists: USeq
lists: NucPosSimulator
lists: NBC
lists: SVMerge
lists: MLTreeMap
lists: SVseq
lists: SEQanswers
lists: PRISM - Pair Read Informed Split Mapper
lists: miRNAKey
lists: MG-RAST
lists: Information Hyperlinked Over Proteins
lists: PubMed
lists: MetaPhyler
lists: MARTA
lists: NCBI BioSample
lists: BioSample Database at EBI
lists: DiScRIBinATE
lists: VariationHunter
lists: NCBI BLAST
lists: IBIS: Inferred Biomolecular Interactions Server
lists: NCBI Sequence Read Archive (SRA)
lists: MetaPhlAn
lists: Classifier for Metagenomic Sequences
lists: MapAl
lists: European Genome phenome Archive
lists: TemplateFilter
lists: Minia
lists: MiTCR
lists: M-pick
lists: CARMA
lists: SLIQ
lists: DNAPlotter
lists: AmphoraNet
lists: UPARSE
lists: SOPRA
lists: ESPRIT-Tree
lists: HPC-CLUST
lists: mirWIP
lists: SSPACE
lists: GoMapMan
lists: G-BLASTN
lists: SINA
lists: Bambus
lists: AGORA
lists: GRASS
lists: MIP Scaffolder
lists: Scarpa
lists: MBCluster.Seq
lists: cortex var
lists: Flux Simulator
lists: BEERS
lists: SNPeffect
lists: MMAPPR
lists: Cloudbreak
lists: comrad
lists: qSNP
lists: SomaticIndelDetector
lists: SomaticSniper
lists: aldex
lists: UnoSeq
lists: Traph
lists: RNA-SeQC
lists: PoPoolation TE
lists: RetroSeq
lists: T-lex
lists: SLIDE
lists: VFS
lists: Project HOPE
lists: PANTHER Evolutionary analysis of coding SNPs
lists: rQuant
lists: Naturejobs
lists: jobs.ac.uk
lists: ASOoViR
lists: RNA-eXpress
lists: MethPipe
lists: AnnTools
lists: AVIA
lists: CandiSNPer
lists: CHAoS
lists: COVA
lists: methylKit
lists: dbNSFP
lists: GESND
lists: VAGrENT
lists: Human Splicing Finder
lists: NGS-SNP
lists: Oncotator
lists: PHAge Search Tool
lists: SCAN
lists: SeqAnt
lists: SNPdat
lists: ORMAN
lists: FRCbam
lists: SNPdbe
lists: SnpEff
lists: SNPnexus
lists: SPOT - Biological prioritization after a SNP association study
lists: VARIANT
lists: ABSOLUTE
lists: ExPANdS
lists: HIVCD
lists: PathSeq
lists: READSCAN
lists: VirusFinder
lists: VirusSeq
lists: PredictHaplo
lists: QuRe
lists: ShoRAH
lists: V-Phaser 2
lists: NSMAP
lists: FlowSim
lists: SimRare
lists: SAMtools/BCFtools
lists: MiTie
lists: GeneTalk
lists: iReckon
lists: Genomic Datasharing
lists: IsoformEx
lists: IQSeq
lists: ERANGE
lists: FusionMap
lists: Bioinformatics(at)school
lists: PhenoMan
lists: Models of SHM Targeting and Substitution
lists: AGE
lists: Breakpointer
lists: CLEVER Toolkit
lists: Clippers
lists: CREST
lists: Indelocator
lists: GASVPro
lists: Hydra
lists: inGAP
lists: VelociMapper
lists: PEMer
lists: SPLITREAD
lists: SpliceSeq
lists: Scripture
lists: Omicsoft Sequence Aligner
lists: SOAPindel
lists: G-Mo.R-Se
lists: SEECER
lists: RSeQC
lists: SeqWare
lists: CloVR
lists: PolySearch
lists: MiRPara
lists: PIE the search
lists: miRdSNP
lists: Hmmer
lists: MuGeX
lists: SysCall
lists: KGGSeq
lists: MycoCosm
lists: EBIMed
lists: HighWire
lists: Coremine Medical
lists: Assembly Likelihood Estimator
lists: CoPub
lists: ABS filter
lists: NCBO Annotator
lists: CHANCE
lists: phantompeakqualtools
lists: CoIN
lists: SwissRegulon
lists: becas
lists: GEM
lists: Anne O'Tate
lists: (at)Note
lists: PeakSeq
lists: FaBox
lists: CoverageCalculator
lists: Spliceman
lists: Yabi
lists: footprintDB
lists: MolBioLib
lists: Moa
lists: PRISM (Stanford database)
lists: Knime4Bio
lists: Ergatis
lists: bioKepler
lists: Platypus
lists: PING
lists: Binding and Expression Target Analysis
lists: BioExtract
lists: Bio-Linux
lists: NeuroLex
lists: ChEA
lists: ChIPBase
lists: CistromeFinder
lists: pyDNase
lists: hmChIP
lists: HOCOMOCO
lists: PAZAR
lists: TFinDIT
lists: AtProbe
lists: DATFAP
lists: StSNP
lists: SolexaQA
lists: TOBFAC
lists: MapNext
lists: BSeQC
lists: SKIPPY
lists: SAMStat
lists: QC-Chain
lists: Bis-SNP
lists: Bisulfighter
lists: CpG MPs
lists: CyMATE
lists: GobyWeb
lists: Kismeth
lists: MethylExtract
lists: MethylViewer
lists: MLML
lists: MSC
lists: PRINSEQ
lists: NGSQC
lists: NGS QC Toolkit
lists: NextClip
lists: Geneious Microsatellite Plugin
lists: DistMap
lists: PRIMEGENS
lists: VDJ
lists: Bowtie
lists: CASHX
lists: CUSHAW
lists: CUSHAW2-GPU
lists: GNUMAP
lists: GSNAP
lists: Kraken
lists: Maq
lists: MOSAIK
lists: mrFAST
lists: NextGenMap
lists: ngsTools
lists: PASS
lists: Jellyfish
lists: TIGRFAMS
lists: Segemehl
lists: SeqMap
lists: SHRiMP
lists: WHAM
lists: SMALT
lists: Scalable Nucleotide Alignment Program
lists: SOAP3
lists: SOAPaligner/soap2
lists: Stampy
lists: TreQ
lists: IdCheck
lists: HTSeq
lists: Hadoop-BAM
lists: MACE
lists: Fulcrum
lists: FreClu
lists: FLASH
lists: FASTX-Toolkit
lists: Hiclib
lists: FastQC
lists: cd-hit-454
lists: CGAT
lists: ea-utils
lists: Genetic Testing Registry
lists: Ridom TraceEdit
lists: HiCUP
lists: TopoSNP
lists: TM4
lists: WebArrayDB
lists: Advanced Sequence Automated Pipeline
lists: Unipro UGENE
lists: SeqTrace
lists: MethylomeDB
lists: FinchTV
lists: DNA Chromatogram Explorer
lists: Chromaseq
lists: OXBench
lists: Sybil
lists: cancergrid-tma
lists: PathXL TMA
lists: Slidepath
lists: Stanford TMA Software
lists: TMA Navigator
lists: TMA-Combiner
lists: TMAJ
lists: X-Tile
lists: Bismark
lists: jMHC
lists: VAGUE
lists: Tractor db
lists: SAMtools Text Alignment Viewer
lists: snp-search
lists: TRANSFAC
lists: Systems Transcriptional Activity Reconstruction
lists: SPOT
lists: LookSeq
lists: Staden Package
lists: Maqview
lists: NGSView
lists: BS Seeker
lists: WISECONDOR
lists: MagicViewer
lists: Bambino
lists: Consed
lists: DiProGB
lists: BSMAP
lists: netClass
lists: BSmooth
lists: DMRforPairs
lists: SeqGSEA
lists: CLIPZ
lists: PePr
lists: MutationAssessor
lists: American College of Medical Genetics and Genomics
lists: Biopieces
lists: SNPsandGO
lists: Unified Human Interactome
lists: OLego
lists: PIPE-CLIP
lists: GoPubMed
lists: SPLINTER
lists: GraphProt
lists: Cascade
lists: PASSion
lists: JEPETTO
lists: dna-bison
lists: aLFQ
lists: BLESS
lists: VirHostNet: Virus-Host Network
lists: CAFE
lists: VirusMINT
lists: GNUMAP-BS
lists: MetaQC
lists: YuGene
lists: h5vc
lists: IQRray
lists: Yeast Search for Transcriptional Regulators And Consensus Tracking
lists: LAST
lists: ScerTF
lists: Tangram
lists: ClinVar
lists: estMOI
lists: FCROS
lists: WashU Epigenome Browser
lists: deepSNV
lists: OMPdb
lists: Rosalind
lists: pepStat
lists: PANOGA
lists: InterSpecies Analysing Application using Containers
lists: GeneTrail
lists: MEDIE
lists: DBM-DB
lists: SpliceDB
lists: RUVSeq
lists: Genomic Standards Consortium
lists: Galaxy
lists: VICUNA
lists: Lists2Networks
lists: PredictSNP
lists: ADGO
lists: KOBAS
lists: GeneTerm Linker
lists: Computational Genomics Analysis Tools
lists: Antibody Registry
lists: BHC
lists: Wigwams
lists: BETASEQ
lists: PhyloBayes
lists: MEGA-MD
lists: CGARS
lists: Magic
lists: epigenomix
lists: QCGWAS
lists: AbsCN-seq
lists: DupRecover
lists: Socrates
lists: CMGRN
lists: SNPdryad
lists: ALEA
lists: MSIsensor
lists: TSSer
lists: IRanges
lists: SILVA
lists: kFM-index
lists: Bioconductor
lists: CHASM/SNV-Box
lists: HTQC
lists: GeneNetworkBuilder
lists: Jalview
lists: SV-M
lists: Hereditary Hearing Loss Homepage
lists: ATRHUNTER
lists: seq crumbs
lists: Google App Engine
lists: COHCAP
lists: MethylSeekR
lists: SAAP-RRBS
lists: targetHub
lists: SRAdb
lists: Picard
lists: NGS-QC Generator
lists: ART
lists: HOMSTRAD - Homologous Structure Alignment Database
lists: DECIPHER
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is related to: COnsensus-DEgenerate Hybride Oligonucleotide Primers
is related to: Classifier for Metagenomic Sequences
is related to: Pedigree-Draw
is related to: CAZy- Carbohydrate Active Enzyme
is related to: PolyPhen: Polymorphism Phenotyping
is related to: BioRAT
is related to: dChip Software
is related to: Rat Genome Database (RGD)
is related to: Comparative Toxicogenomics Database (CTD)
is related to: VISTA Enhancer Browser
is related to: affy
PMID:25024350 THIS RESOURCE IS NO LONGER IN SERVICE nlx_155571, r3d100012426 https://doi.org/10.17616/R3PJ3N http://omictools.com/ SCR_002250 genOMIC tools 2026-02-16 09:45:41 34
SNAP - SNP Annotation and Proxy Search
 
Resource Report
Resource Website
100+ mentions
SNAP - SNP Annotation and Proxy Search (RRID:SCR_002127) SNAP software application, data analysis service, analysis service resource, software resource, production service resource, service resource A computer program and web-based service for the rapid retrieval of linkage disequilibrium proxy single nucleotide polymorphism (SNP) results given input of one or more query SNPs and based on empirical observations from the International HapMap Project and the 1000 Genomes Project. A series of filters allow users to optionally retrieve results that are limited to specific combinations of genotyping platforms, above specified pairwise r2 thresholds, or up to a maximum distance between query and proxy SNPs. SNAP can also generate linkage disequilibrium plots gene, genetic, genomic, r, oracle, single nucleotide polymorphism, linkage disequilibrium, genotypeing array, physical distance, membership, proxy, plot is listed by: OMICtools
is listed by: Genetic Analysis Software
is related to: International HapMap Project
is related to: 1000 Genomes: A Deep Catalog of Human Genetic Variation
has parent organization: Broad Institute
NHLBI N01-HC-65226 PMID:18974171 Free, Freely Available OMICS_01927, nlx_154638 http://www.broad.mit.edu/mpg/snap/ SCR_002127 SNAP (SNP Annotation and Proxy Search), SNAP 2, SNP Annotation and Proxy Search 2026-02-16 09:45:44 144
Protein Structure Initiative
 
Resource Report
Resource Website
Protein Structure Initiative (RRID:SCR_002161) data or information resource, topical portal, portal The Structural Genomics Project aims at determination of the 3D structure of all proteins. It also aims to reduce the cost and time required to determine three-dimensional protein structures. It supports selection, registration, and tracking of protein families and representative targets. This aim can be achieved in four steps : -Organize known protein sequences into families. -Select family representatives as targets. -Solve the 3D structure of targets by X-ray crystallography or NMR spectroscopy. -Build models for other proteins by homology to solved 3D structures. PSI has established a high-throughput structure determination pipeline focused on eukaryotic proteins. NMR spectroscopy is an integral part of this pipeline, both as a method for structure determinations and as a means for screening proteins for stable structure. Because computational approaches have estimated that many eukaryotic proteins are highly disordered, about 1 year into the project, CESG began to use an algorithm. The project has been organized into two separate phases. The first phase was dedicated to demonstrating the feasibility of high-throughput structure determination, solving unique protein structures, and preparing for a subsequent production phase. The second phase, PSI-2, has focused on implementing the high-throughput structure determination methods developed in PSI-1, as well as homology modeling and addressing bottlenecks like modeling membrane proteins. The first phase of the Protein Structure Initiative (PSI-1) saw the establishment of nine pilot centers focusing on structural genomics studies of a range of organisms, including Arabidopsis thaliana, Caenorhabditis elegans and Mycobacterium tuberculosis. During this five-year period over 1,100 protein structures were determined, over 700 of which were classified as unique due to their < 30% sequence similarity with other known protein structures. The primary goal of PSI-1 was to develop methods to streamline the structure determination process, resulted in an array of technical advances. Several methods developed during PSI-1 enhanced expression of recombinant proteins in systems like Escherichia coli, Pichia pastoris and insect cell lines. New streamlined approaches to cell cloning, expression and protein purification were also introduced, in which robotics and software platforms were integrated into the protein production pipeline to minimize required manpower, increase speed, and lower costs. The goal of the second phase of the Protein Structure Initiative (PSI-2) is to use methods introduced in PSI-1 to determine a large number of proteins and continue development in streamlining the structural genomics pipeline. Currently, the third phase of the PSI is being developed and will be called PSI: Biology. The consortia will propose work on substantial biological problems that can benefit from the determination of many protein structures Sponsors: PSI is funded by the U.S. National Institute of General Medical Sciences (NIGMS), elegans, escherichia, eukaryotic, expression, arabidopsis, biology, bottleneck, caenorhabditis, cell, clone, coli, crystallography, genomic, homology, insect, membrane, myobacterium, nmr, organism, pastoris, pichia, protein, purification, sequence, spectroscopy, structural, structure, thaliana, tuberculosis, x-ray nif-0000-20950 SCR_002161 PSI 2026-02-16 09:45:42 0
QGene
 
Resource Report
Resource Website
100+ mentions
QGene (RRID:SCR_003209) QGene software application, data processing software, data analysis software, source code, software resource, simulation software A free, open-source, computationally efficient Java program for comparative analyses of QTL mapping data and population simulation that runs on any computer operating system. (entry from Genetic Analysis Software) It is written with a plug-in architecture for ready extensibility. The software accommodates line-cross mating designs consisting of any arbitrary sequence of selfing, backcrossing, intercrossing and haploid-doubling steps that includes map, population, and trait simulators; and is scriptable. Source code is available on request. gene, genetic, genomic, java, qtl mapping, trait analysis, trait, population, simulation, map, quantitative trait locus, comparison, bio.tools is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
has parent organization: Kansas State University; Kansas; USA
NSF DBI 0109879;
USDA-NRI Applied Plant Genomics Program 2004-35317-14867
PMID:18940826 Free, Available for download, Freely available biotools:qgene, nif-0000-31383 https://bio.tools/qgene http://coding.plantpath.ksu.edu/qgene SCR_003209 QGene - Software for QTL data exploration 2026-02-16 09:46:02 126
MGH-USC Human Connectome Project
 
Resource Report
Resource Website
100+ mentions
MGH-USC Human Connectome Project (RRID:SCR_003490) MGH/UCLA HCP material service resource, instrument manufacture, portal, production service resource, service resource, data or information resource A multi-center project comprising two distinct consortia (Mass. Gen. Hosp. and USC; and Wash. U. and the U. of Minn.) seeking to map white matter fiber pathways in the human brain using leading edge neuroimaging methods, genomics, architectonics, mathematical approaches, informatics, and interactive visualization. The mapping of the complete structural and functional neural connections in vivo within and across individuals provides unparalleled compilation of neural data, an interface to graphically navigate this data and the opportunity to achieve conclusions about the living human brain. The HCP is being developed to employ advanced neuroimaging methods, and to construct an extensive informatics infrastructure to link these data and connectivity models to detailed phenomic and genomic data, building upon existing multidisciplinary and collaborative efforts currently underway. Working with other HCP partners based at Washington University in St. Louis they will provide rich data, essential imaging protocols, and sophisticated connectivity analysis tools for the neuroscience community. This project is working to achieve the following: 1) develop sophisticated tools to process high-angular diffusion (HARDI) and diffusion spectrum imaging (DSI) from normal individuals to provide the foundation for the detailed mapping of the human connectome; 2) optimize advanced high-field imaging technologies and neurocognitive tests to map the human connectome; 3) collect connectomic, behavioral, and genotype data using optimized methods in a representative sample of normal subjects; 4) design and deploy a robust, web-based informatics infrastructure, 5) develop and disseminate data acquisition and analysis, educational, and training outreach materials. human, structural, functional, neural, white matter, fiber, brain, in vivo, genomic, neuroimaging, visualization, neuroanatomy, genotype, connectivity, connectivity model, neural pathway, phenomic, connectomics, quantification, scanner, eeg, meg, shape analysis, spatial transformation, diffusion spectrum, q-ball, tensor metric, fiber tracking, connectome, behavior, scanner, web resource, diffusion spectrum, q-ball, tensor metric, quantification, shape analysis, spatial transformation, fiber tracking, FASEB list is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Biositemaps
has parent organization: Laboratory of Neuro Imaging
has parent organization: Harvard Medical School; Massachusetts; USA
has parent organization: NIH Human Connectome Project
is parent organization of: USC Multimodal Connectivity Database
Normal NIH ;
NIH Blueprint for Neuroscience Research
Open unspecified license, (BSD/MIT-Style), LONI Software License, Public Domain nif-0000-35789 http://www.nitrc.org/projects/hcp_mgh-ucla SCR_003490 Harvard/MGH-UCLA Human Connectome Project, Harvard/MGH-UCLA Consortium: Human Connectome Project, HCP Harvard/MGH-UCLA, MGH/UCLA Consortium: Human Connectome Project 2026-02-16 09:46:13 165
Eutherian comparative genomic analysis protocol
 
Resource Report
Resource Website
10+ mentions
Eutherian comparative genomic analysis protocol (RRID:SCR_014401) data set, data or information resource, protocol Eutherian comparative genomic analysis protocol as one framework of eutherian gene data set revisions. Protocol integrated gene annotations, phylogenetic analysis and protein molecular evolution analysis with 3 new tests including test of reliability of public eutherian genomic sequences using genomic sequence redundancies, test of contiguity of public eutherian genomic sequences using multiple pairwise genomic sequence alignments and test of protein molecular evolution using relative synonymous codon usage statistics. Public eutherian reference genomic sequence data sets. eutheria, gene, data set, annotation, genomic, molecular, evolution, phylogenetic, analysis protocol has parent organization: Australian National University; Acton; Australia
works with: European Nucleotide Archive (ENA)
DOI:10.1016/j.genrep.2019.100414 Free, Freely available https://doi.org/10.1016/j.dib.2015.11.056 SCR_014401 2026-02-16 09:48:34 15

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