Data Science & Analytics
Pysam
Genomic file toolkit. For reading/writing SAM/BAM/CRAM alignment files, VCF/BCF variant files, FASTA/FASTQ sequences, extracting regions, calculating coverage, suitable for NGS data processing pipelines.
- Publisher / source
- aipoch/medical-research-skills (found on GitHub top repositories)
- Upstream record
- aipoch/medical-research-skills
- Version
- Version 1
- Published
- Publication review
- Approved for publication
- Content fingerprint
77658f424d8d38bbd03a15c5de98034dae6ca52fbf91a4ed1006956f33d17136