lynnlangit / AdvancedPythonForBioLinks
Work from the book 'Advanced Python for Biologists'
☆12Updated 7 years ago
Alternatives and similar repositories for AdvancedPythonForBio
Users that are interested in AdvancedPythonForBio are comparing it to the libraries listed below
Sorting:
- Sphinx documentation source for a computational genomics tutorial.☆36Updated 5 years ago
- A repository for my solutions to problems from - http://www.rosalind.info☆23Updated 4 years ago
- ☆20Updated 5 years ago
- NGS-1 Data analysis course☆38Updated 4 years ago
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆40Updated 4 months ago
- Website for the precision medicine workshop☆46Updated 2 months ago
- This repository contains course materials from JAX-BD2K workshop.☆32Updated 6 years ago
- The wiki repo, with pull request enabled, for the rnaseq_tutorial☆26Updated 5 years ago
- ☆15Updated 3 years ago
- GATK4 Best Practice Nextflow Pipeline☆33Updated 8 years ago
- ☆19Updated last year
- Code and custom scripts relevant to gnomAD-SV (Collins*, Brand*, et al., 2020)☆37Updated 5 years ago
- GitHub for the SIB courses NGS - Genome variant analysis☆27Updated this week
- Applied Python Programming for Life Scientists☆26Updated 4 years ago
- CRUK Bioinformatics Workshop September 2017☆18Updated 8 years ago
- practical course about lab methods in genome research☆23Updated 3 years ago
- Scripts, utilities and programs for genomic bioinformatics.☆83Updated 2 months ago
- Rosalind Bioinformatics Problems☆32Updated 10 years ago
- Bioinformatics analysis scripts, workflows, general code examples☆54Updated 4 years ago
- Scripts for bioinformatics data processing and analysis☆12Updated 2 years ago
- Germline Variant Calling Nextflow Pipeline Based On GATK4 Best Practices☆11Updated 5 years ago
- Generic human DNA variant annotation pipeline☆59Updated last year
- repository of scripts for comparative transcriptome analysis☆19Updated 6 years ago
- For biological deep sequencing data. Decompose a UCSC knownGenes/Ensembl GTF file into transcript regions (i.e. exons, introns, UTRs and…☆36Updated 2 years ago
- Workflows for germline short variant discovery in WGS data. PairedEndSingleSampleWf has been superseded in Broad production by https://gi…☆57Updated 5 years ago
- GWAS QC, PCA, haplotype phasing, genotype imputation☆20Updated 5 months ago
- A python package and a set of shell commands to handle GTF files☆50Updated last month
- Web-site for the 2020 CRUK CC Bioinformatics Summer School (Held virtually)☆24Updated 4 years ago
- Bioinformatics one-liner for 100 days☆49Updated last year
- HPC based pipelines for variant calling using GATK☆17Updated 5 years ago