Generate consensus reads to reduce sequencing noises and remove duplications

⛏HLA predictions from NGS shotgun data

Fork of the Polysolver project

R Package for Non Invasive Prenatal Testing (NIPT) analysis

In-silico method written in Python and R to determine HLA genotypes of a sample. seq2HLA takes standard RNA-Seq sequence reads in fastq format as input, uses a bowtie index comprising all HLA allel…

lumpy: a general probabilistic framework for structural variant discovery

Assign gene names to regions in a BED file

Tools to process LIANTI sequence data

利用Python进行数据分析 第二版 (2017) 中文翻译笔记

cart analysis

A flexible framework for rapid genome analysis and interpretation

A microframework based on Werkzeug, Jinja2 and good intentions