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Submitted URL: http://htslib.org/
Effective URL: https://www.htslib.org/
Submission Tags: tranco_l324
Submission: On May 20 via api from DE — Scanned from GB
Effective URL: https://www.htslib.org/
Submission Tags: tranco_l324
Submission: On May 20 via api from DE — Scanned from GB
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Toggle navigation Samtools * Home * Download * Downloads * Development * Workflows * FASTQ to BAM / CRAM * WGS/WES Mapping to Variant Calls * Filtering of VCF Files * Using CRAM within Samtools * Documentation * Man Pages * HowTos * Specifications * Duplicate Marking * Zlib Benchmarks * CRAM Benchmarks * Publications * Support * Mailing Lists * HTSlib issues * BCFtools issues * Samtools issues SAMTOOLS Samtools is a suite of programs for interacting with high-throughput sequencing data. It consists of three separate repositories: Samtools Reading/writing/editing/indexing/viewing SAM/BAM/CRAM format BCFtools Reading/writing BCF2/VCF/gVCF files and calling/filtering/summarising SNP and short indel sequence variants HTSlib A C library for reading/writing high-throughput sequencing data Samtools and BCFtools both use HTSlib internally, but these source packages contain their own copies of htslib so they can be built independently. DOWNLOAD Source code releases can be downloaded from GitHub or Sourceforge: Source release details WORKFLOWS We have described some standard workflows using Samtools: * FASTQ to BAM / CRAM * WGS/WES Mapping to Variant Calls * Filtering of VCF Files * Using CRAM within Samtools DOCUMENTATION * Manuals * HowTos * Specifications * Duplicate Marking * Zlib Benchmarks * CRAM Benchmarks * Publications SUPPORT * Mailing Lists * HTSlib issues * BCFtools issues * Samtools issues -------------------------------------------------------------------------------- Copyright © 2023 Genome Research Limited (reg no. 2742969) is a charity registered in England with number 1021457. Terms and conditions.