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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 Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
pysam
 
Resource Report
Resource Website
100+ mentions
pysam (RRID:SCR_021017) software resource, software toolkit Software tool as interface for reading and writing SAM files. Python module to read and manipulate mapped short read sequence data stored in SAM/BAM files. Lightweight wrapper of htslib C-API. Interface, reading SAM files, writing SAM files, mapped short read sequence data, htslib C-API wrapper, SAM/BAM files is related to: SAMTOOLS
is related to: SAM
Free, Available for download, Freely available https://github.com/pysam-developers/pysam SCR_021017 2026-08-08 12:05:29 164
SAMTOOLS
 
Resource Report
Resource Website
10000+ mentions
SAMTOOLS (RRID:SCR_002105) SAMtools sequence analysis software, software toolkit, software resource, software application, data analysis software, data processing software Original SAMTOOLS package has been split into three separate repositories including Samtools, BCFtools and HTSlib. Samtools for manipulating next generation sequencing data used for reading, writing, editing, indexing,viewing nucleotide alignments in SAM,BAM,CRAM format. BCFtools used for reading, writing BCF2,VCF, gVCF files and calling, filtering, summarising SNP and short indel sequence variants. HTSlib used for reading, writing high throughput sequencing data. Samtools, BCFtools, HTSlib, next generation sequencing, nucleotide alignments, sequence variant, genomic, c, perl, read, alignment, nucleotide, sequence, data, process, sam, bam, cram, vcf, bcf, bio.tools is used by: deFuse
is used by: Short Read Sequence Typing for Bacterial Pathogens
is used by: ROSE
is used by: Fcirc
is listed by: OMICtools
is listed by: Genetic Analysis Software
is listed by: SNVer
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
is related to: Platypus
is related to: shovill
is related to: pysam
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
is parent organization of: SAMtools/BCFtools
is required by: RelocaTE
is required by: Wessim
is required by: SL-quant
is required by: smMIPfil
Wellcome Trust ;
NHGRI U54 HG002750
PMID:19505943
PMID:21903627
DOI:10.1093/bioinformatics/btp352
Free, Available for download, Freely available SCR_018682, biotools:samtools, OMICS_01074, nlx_154607, OMICS_00090 https://github.com/samtools/samtools, https://github.com/samtools/htslib, https://bio.tools/samtools, https://sources.debian.org/src/samtools/ http://samtools.sourceforge.net/ SCR_002105 samtools, Samtools, Sequence Alignment Map TOOLS, SAMtools, SAM tools 2026-08-08 11:57:47 33299
SAM
 
Resource Report
Resource Website
100+ mentions
SAM (RRID:SCR_010951) software resource Software for genomic expression data mining using a statistical technique for finding significant genes in a set of microarray experiments. genomic expression, data mining, finding significant genes, microarray experiments, is listed by: OMICtools
is listed by: Debian
is listed by: SoftCite
is related to: pysam
has parent organization: Stanford University; Stanford; California
Commercial use requires license, Registration required OMICS_01314, OMICS_00779, SCR_011888 https://sources.debian.org/src/r-cran-samr/ SCR_010951 SAM: Significance Analysis of Microarrays, Significance Analysis of Microarrays 2026-08-08 12:05:58 235

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