Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis
created at Feb. 6, 2013, 11:14 a.m.
RNAseq analysis notes from Ming Tang
created at Aug. 26, 2015, 7:37 p.m.
De novo assembler for single molecule sequencing reads using repeat graphs
created at March 17, 2016, 10:47 p.m.
Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight wrapper of the HTSlib API, the same one that powers samtools, bcftools, and tabix.
created at Feb. 5, 2014, 8:38 p.m.
ChIP-seq analysis notes from Ming Tang
created at June 12, 2015, 9:42 p.m.