pejvan / Algorithms-for-DNA-Sequencing
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
- Student website repo for 2015/2016 Canadian Bioinformatics Workshops☆34Updated last year
- A repository for my solutions to problems from - http://www.rosalind.info☆21Updated 3 years ago
- Breakpoints via assembly - Identifies breaks and attempts to assemble rearrangements in whole genome sequencing data.☆57Updated 7 months ago
- Workflows for converting between sequence data formats☆38Updated 3 years ago
- Next-Generation Sequencing(NGS) toolkits.☆45Updated 8 years ago
- Issue tracker for the Biostar Handbook☆61Updated 2 years ago
- A simple variant calling and annotation pipeline using BWA, GATK and ENSEMBL. This version of the pipeline uses the Rubra/Ruffus framewor…☆33Updated 10 years ago
- Materials for Spring 2018 Applied Genomics Course☆78Updated 6 years ago
- Bioinformatics analysis scripts, workflows, general code examples☆53Updated 4 years ago
- Scripts, utilities and programs for genomic bioinformatics.☆81Updated last week
- Tutorials on accessing public reference and genomic data☆31Updated this week
- The wiki repo, with pull request enabled, for the rnaseq_tutorial☆26Updated 4 years ago
- This repo has been archived, these workflows are still available in the GATK repository under the scripts directory. The workflows are al…☆77Updated 4 years ago
- ☆48Updated 3 years ago
- Python for Genomic Data Science 2015 Coursera from Johns Hopkins University☆17Updated 9 years ago
- Multi-sample somatic variant caller☆49Updated 3 years ago
- Automatically exported from code.google.com/p/ea-utils☆95Updated last year
- New user☆42Updated 4 years ago
- CRT outreach program to assist life scientists in learning basic data science skills.☆28Updated 4 years ago
- Learning the Variant Call Format☆138Updated 10 months ago
- Scripts for next generation sequencing☆48Updated 5 years ago
- Documenting usage and experience with bioinformatic tools☆41Updated 9 years ago
- Julia package powering VIVA, our tool for visualization of genomic variation data. Manual:☆85Updated last year
- NGS-pipe: next-generation sequencing pipelines for precision oncology☆109Updated 6 years ago
- Identifying recurrent mutations in cancer☆37Updated 3 years ago
- Generic human DNA variant annotation pipeline☆57Updated last year
- This WDL pipeline implements data pre-processing and initial variant calling according to the GATK Best Practices for germline SNP and In…☆52Updated 4 years ago
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆76Updated 2 months ago
- ☆66Updated last year
- ☆25Updated 2 months ago