pejvan / Algorithms-for-DNA-SequencingLinks
Coursera MOOC Algorithms for DNA Sequencing by Ben Langmead, PhD, Jacob Pritt
☆13Updated 9 years ago
Alternatives and similar repositories for Algorithms-for-DNA-Sequencing
Users that are interested in Algorithms-for-DNA-Sequencing are comparing it to the libraries listed below
Sorting:
- website for the rnaseq course☆109Updated last month
- Issue tracker for the Biostar Handbook☆64Updated 3 years ago
- Materials for Spring 2018 Applied Genomics Course☆79Updated 6 years ago
- Training requirements for joining projects☆80Updated last year
- Scripts and data for Plotting in R for Biologists, a video course on YouTube☆61Updated 5 years ago
- materials for the RNA-Seq workshop on Trinity and Tuxedo, covering de novo and genome-guided transcript assembly and downstream analysis.☆48Updated 9 years ago
- A repository for my solutions to problems from - http://www.rosalind.info☆22Updated 4 years ago
- A proof of concept of RNAseq pipeline☆79Updated last week
- New user☆42Updated 5 years ago
- Learning the Variant Call Format☆144Updated 2 months ago
- NGS-pipe: next-generation sequencing pipelines for precision oncology☆114Updated 6 years ago
- Scripts, utilities and programs for genomic bioinformatics.☆83Updated last month
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 5 years ago
- Sphinx documentation source for a computational genomics tutorial.☆34Updated 4 years ago
- Source code and related materials for the O'Reilly book☆96Updated 3 years ago
- ☆28Updated 3 weeks ago
- Workflows for germline short variant discovery in WGS data. PairedEndSingleSampleWf has been superseded in Broad production by https://gi…☆56Updated 5 years ago
- Crash course for NCBI blast tools☆44Updated 6 years ago
- Materials for 12-day course on analyzing RNA-Seq, ChIP-Seq and variant calling data.☆16Updated 6 years ago
- The wiki repo, with pull request enabled, for the rnaseq_tutorial☆26Updated 5 years ago
- Breakpoints via assembly - Identifies breaks and attempts to assemble rearrangements in whole genome sequencing data.☆57Updated last year
- ☆50Updated 4 years ago
- Next-Generation Sequencing(NGS) toolkits.☆48Updated 9 years ago
- A simple variant calling and annotation pipeline using BWA, GATK and ENSEMBL. This version of the pipeline uses the Rubra/Ruffus framewor…☆34Updated 11 years ago
- ☆73Updated 3 years ago
- Intro to Shell for Bioinformatics - with STG examples☆28Updated 9 years ago
- Bioinformatics and genomics resources☆78Updated 2 months ago
- R package designed to simplify structural variant analysis☆73Updated 3 years ago
- GWAS Pipeline for H3Africa☆113Updated 4 months ago
- RNA-seq workflow: exploratory analysis and differential expression☆80Updated last year