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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
Sequencing Analysis Software
 
Resource Report
Resource Website
1+ mentions
Sequencing Analysis Software (RRID:SCR_000718) Sequencing Analysis Software software resource A software that gives the user the ability to basecall, trim, display, edit, and print data for the entire line of capillary DNA sequencing instruments for data analysis and quality control. This software benefits from being able to obtain longer read lengths, greater accuracy on the 5' end, and the ability to filter out low-quality sequence ends. basecall, capillary dna, quality control, low-quality sequence ends is listed by: OMICtools Restricted OMICS_01814 SCR_000718 2026-02-14 01:59:52 1
clipcrop
 
Resource Report
Resource Website
clipcrop (RRID:SCR_000678) software resource Software tool for detecting structural variations with single-base resolution using soft-clipping information from SAM files. structural variation, detecting structural variations, soft-clipping information, SAM files, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:22373054 Free, Available for download, Freely available biotools:clipcrop, OMICS_00310 https://bio.tools/clipcrop SCR_000678 ClipCrop 2026-02-14 01:59:48 0
TriageTools
 
Resource Report
Resource Website
TriageTools (RRID:SCR_000675) TriageTools software resource A collection of tools for partitioning raw data (fastq reads) from high-throughput sequencing projects. The tools are designed for basic data management as well for prioritizing analysis of certain subsets. matlab, java, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:23408855 Free, Available for download, Freely available biotools:triagetools, nlx_156740 https://bio.tools/triagetools SCR_000675 2026-02-14 01:59:48 0
VarB
 
Resource Report
Resource Website
VarB (RRID:SCR_000671) VarB software resource A variation browsing and analysis tool for variants derived from next-generation sequencing data. variant, next-generation sequencing, polymorphism, c++ is listed by: OMICtools PMID:22976080 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00898 SCR_000671 2026-02-14 01:59:51 0
MSG
 
Resource Report
Resource Website
1+ mentions
MSG (RRID:SCR_004161) MSG software resource A pipeline of scripts to assign ancestry to genomic segments using next-gen sequence data. This method can identify recombination breakpoints in a large number of individuals simultaneously at a resolution sufficient for most mapping purposes, such as quantitative trait locus (QTL) mapping and mapping of induced mutations. next generation sequencing, genotyping, genetic mapping, ancestry, genome is listed by: OMICtools
has parent organization: Princeton University; New Jersey; USA
PMID:21233398 OMICS_01551 SCR_004161 Multiplexed shotgun genotyping, Multiplexed shotgun genotyping (MSG), MSG: Multiplexed Shotgun Genotyping 2026-02-14 02:00:41 2
PerM
 
Resource Report
Resource Website
50+ mentions
PerM (RRID:SCR_004223) software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on February 28,2023. Software package to perform highly efficient genome scale alignments for hundreds of millions of short reads produced by the ABI SOLiD and Illumina sequencing platforms. It capable of providing full sensitivity for alignments within 4 mismatches for 50bp SOLID reads and 9 mismatches for 100bp Illumina reads.Efficient mapping of short sequencing reads with periodic full sensitive spaced seeds. Short sequencing mapping, short sequencing read, next-generation sequencing, genome, alignment, short read, abi, solid, illumina, , bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Clippers
has parent organization: Google Code
has parent organization: University of Southern California; Los Angeles; USA
PMID:19675096
DOI:10.1093/bioinformatics/btp486
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00675, biotools:perm https://bio.tools/perm
https://sources.debian.org/src/perm/
SCR_004223 PERiodic seed Mapping, Periodic seed Mapping 2026-02-14 02:00:38 60
HLASeq
 
Resource Report
Resource Website
HLASeq (RRID:SCR_004185) HLASeq software resource An open-source software tool for accurate genotyping the human HLA genes from Illumina GA high-throughput sequencing data. genotyping, hla, next generation sequencing, gene, command-line, python is listed by: OMICtools
has parent organization: SourceForge
GNU General Public License, v3 OMICS_01543 SCR_004185 2026-02-14 02:00:38 0
PASS-bis
 
Resource Report
Resource Website
PASS-bis (RRID:SCR_004176) PASS-bis software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 9, 2023. A bisulfite aligner suitable for whole methylome analysis of Illumina and SOLiD reads. is listed by: OMICtools
is related to: PASS
PMID:23162053 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00587 SCR_004176 2026-02-14 02:00:55 0
DRUT
 
Resource Report
Resource Website
DRUT (RRID:SCR_004351) DRUT software resource Software for Discovery and Reconstruction of Unannotated Transcripts in Partially Annotated Genomes from High-Throughput RNA-Seq Data. c++, reconstruction, frequency estimation, transcript, rna-seq, annotation is listed by: OMICtools
has parent organization: Georgia State University; Georgia; USA
NSF IIS-0546457;
NSF IIS-0916401;
NSF IIS-0916948
PMID:23202426 OMICS_01273 SCR_004351 Discovery and Reconstruction of Unannotated Transcripts 2026-02-14 02:00:57 0
ACT: Artemis Comparison Tool
 
Resource Report
Resource Website
10+ mentions
ACT: Artemis Comparison Tool (RRID:SCR_004507) ACT software resource A free tool for displaying pairwise comparisons between two or more DNA sequences. It can be used to identify and analyze regions of similarity and difference between genomes and to explore conservation of synteny, in the context of the entire sequences and their annotation. It is based on the software for Artemis, the genome viewer and annotation tool. ACT runs on UNIX, GNU/Linux, Macintosh and MS Windows systems. It can read complete EMBL and GENBANK entries or sequences in FASTA or raw format. Other sequence features can be in EMBL, GENBANK or GFF format. dna sequence, genome, synteny, pairwise comparison is listed by: OMICtools
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
Wellcome Trust PMID:15976072 GNU General Public License OMICS_00928, nlx_48986 SCR_004507 Artemis Comparison Tool 2026-02-14 02:00:44 46
Squeezambler
 
Resource Report
Resource Website
Squeezambler (RRID:SCR_004385) Squeezambler software resource Software to sequence and de novo assemble all distinct genomes present in a microbial sample with a sequencing cost and computational complexity proportional to the number of genome types, rather than the number of cells. is listed by: OMICtools
has parent organization: Wayne State University; Michigan; USA
PMID:23918251 OMICS_01503 SCR_004385 2026-02-14 02:00:56 0
SNiPer-HD
 
Resource Report
Resource Website
1+ mentions
SNiPer-HD (RRID:SCR_004383) SNiPer-HD software resource Improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays. is listed by: OMICtools PMID:17062589 OMICS_00735 SCR_004383 SNiPer-HD: Improved genotype calling accuracy 2026-02-14 02:00:58 2
Vanator
 
Resource Report
Resource Website
1+ mentions
Vanator (RRID:SCR_004370) Vanator software resource A Perl pipeline utilising a large variety of common alignment, assembly and analysis tools to assess the metagenomic profiles of Illumina deep sequencing samples. The emphasis is on the discovery of novel viruses in clinical and environmental samples. perl, metagenomic, illumina, alignment, assembly, analysis, profile, virus, clinical, environment, next-generation sequencing, taxonomy, read is listed by: OMICtools
has parent organization: SourceForge
has parent organization: University of Glasgow; Glasgow; United Kingdom
PMID:23296970 OMICS_01505 SCR_004370 Vanator-CVR, Vanator-CVR - A metagenomics & virus discovery pipeline, Virus Alignment de Novo Assembly and Taxonomy On Reads, Vanator-CVR: A metagenomics and virus discovery pipeline 2026-02-14 02:00:58 2
Basic OligoNucleotide Design
 
Resource Report
Resource Website
10+ mentions
Basic OligoNucleotide Design (RRID:SCR_004492) BOND software resource Software program to compute highly specific DNA oligonucleotides, for all the genes that admit unique probes, while running orders of magnitude faster than the existing programs. dna, oligonucleotide, design, oligonucleotide design is listed by: OMICtools
has parent organization: Western University; Ontario; Canada
PMID:23444904 OMICS_00827 SCR_004492 BOND: Basic OligoNucleotide Design 2026-02-14 02:00:57 17
SOrt-ITEMS
 
Resource Report
Resource Website
1+ mentions
SOrt-ITEMS (RRID:SCR_004716) SOrt-ITEMS software resource Sequence orthology based software for improved taxonomic estimation of metagenomic sequences., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. metagenome, taxonomy, sequence, orthology, binning is listed by: OMICtools PMID:19439565 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01465 SCR_004716 Sequence orthology based approach for improved taxonomic estimation of metagenomic sequences, SOrt-ITEMS: Sequence orthology based approach for improved taxonomic estimation of metagenomic sequences 2026-02-14 02:00:46 6
UnifiedGenotyper
 
Resource Report
Resource Website
500+ mentions
UnifiedGenotyper (RRID:SCR_004710) UnifiedGenotyper software resource A multiple-sample, technology-aware SNP and indel caller. is listed by: OMICtools
has parent organization: Broad Institute
OMICS_00080 SCR_004710 2026-02-14 02:00:59 561
NuChart
 
Resource Report
Resource Website
1+ mentions
NuChart (RRID:SCR_004703) NuChart software resource An R Package to Study Gene Spatial Neighbourhoods with Multi-Omics Annotations. is listed by: OMICtools OMICS_00525 SCR_004703 2026-02-14 02:00:43 2
Pplacer
 
Resource Report
Resource Website
10+ mentions
Pplacer (RRID:SCR_004737) Pplacer software resource Software that places query sequences on a fixed reference phylogenetic tree to maximize phylogenetic likelihood or posterior probability according to a reference alignment. Pplacer is designed to be fast, to give useful information about uncertainty, and to offer advanced visualization and downstream analysis. classification, phylogenetic classification is listed by: OMICtools
has parent organization: Fred Hutchinson Cancer Center
PMID:21034504 OMICS_01462 SCR_004737 pplacer: phylogenetic placement and downstream analysis 2026-02-14 02:00:44 30
TETRA
 
Resource Report
Resource Website
50+ mentions
TETRA (RRID:SCR_004573) TETRA software resource Standalone software programs that can be used to calculate how well tetranucleotide usage patterns in DNA sequences correlate. Such correlations can provide valuable hints on the relatedness of DNA sequences. tetranucleotide, dna sequence is listed by: OMICtools
has parent organization: Max Planck Institute for Marine Microbiology; Bremen; Germany
PMID:15305919
PMID:15507136
OMICS_01474 SCR_004573 TETRA - Fragment assignment by intrinsic tetranucleotide frequencies 2026-02-14 02:00:42 67
BioPig
 
Resource Report
Resource Website
1+ mentions
BioPig (RRID:SCR_004636) BioPig software resource Software providing a framework for genomic data analysis using Apache Pig and Hadoop. mapreduce/hadoop, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Lawrence Berkeley National Laboratory
PMID:24021384 biotools:biopig, OMICS_01225 https://bio.tools/biopig SCR_004636 2026-02-14 02:00:58 2

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