C++ htslib/bwa-mem/fermi interface for interrogating sequence data
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Updated
Aug 9, 2024 - C++
C++ htslib/bwa-mem/fermi interface for interrogating sequence data
BWA-MEME: Faster BWA-MEM2 using learned-index
Here we are going to discuss variant calling on human datasets using GATK Best practices pipeline
Sentieon DNAseq
Optimised pipeline to process whole genome sequence data from fastq to BAM on NCI Gadi
Detecting transposable element invasions without repeat library. Detects also horizontal transfer events and endogenized viruses. All you need is a reference genome and some short reads
The DKFZ alignment workflow plugin originally developed at the eilslabs
vSNP -- validate SNPs
Collecting Genotypes from ENA and make their SNPs
Small GATK alignment and variant calling pipeline using python
This repository will house the scripts used to analyze and represent genomic and temperature data for my dissertation.
Fast bwa-mem dna matching algor implemented in system verilog, fully synthesizable.
The second part of https://github.com/npanuhin/BIOCAD
Multi-class classification of drug resistance in MTB clinical isolates
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