KennethJHan / Genome-Analysis-TutorialLinks
The Genome Analysis Tutorial Page.
☆13Updated 6 years ago
Alternatives and similar repositories for Genome-Analysis-Tutorial
Users that are interested in Genome-Analysis-Tutorial are comparing it to the libraries listed below
Sorting:
- Learning the Variant Call Format☆147Updated 5 months ago
- FRASER - Find RAre Splicing Events in RNA-seq☆52Updated 3 months ago
- 유전학자를 위한 시퀀싱 자료 분석☆23Updated 5 years ago
- Materials for Spring 2018 Applied Genomics Course☆79Updated 7 years ago
- Analysis pipelines for genomic sequencing data☆72Updated this week
- Practical Deep Learning for Genomic Prediction: A Keras based guide to implement deep learning☆69Updated 2 years ago
- website for the rnaseq course☆117Updated last month
- Characterization of Germline variants☆99Updated 3 years ago
- Scripts to run copynumber variation calls on tumor and normal BAM files using Varscan2☆30Updated 7 years ago
- optimization of ribosome P-site positioning in ribosome profiling data☆59Updated 11 months ago
- ☆57Updated last week
- A tutorial in Python where all the examples teach students about biology. Written for high school students with no previous experience.☆19Updated 10 years ago
- ☆18Updated 3 years ago
- Portable eQTL analysis and statistical fine mapping workflow used by the eQTL Catalogue☆57Updated 4 months ago
- ☆74Updated 2 years ago
- Bioinformatics and genomics resources☆83Updated 3 weeks ago
- Personal notes about work- and coding-related topics☆21Updated 2 years ago
- SigProfilerMatrixGenerator creates mutational matrices for all types of somatic mutations. It allows downsizing the generated mutations o…☆116Updated this week
- NGS-pipe: next-generation sequencing pipelines for precision oncology☆114Updated 6 years ago
- Genome-wide Association Study (GWAS) Tutorial☆40Updated 6 years ago
- Integrate DNA-seq and RNA-seq data to identify mutations that are associated with regulatory effects on gene expression.☆136Updated last year
- Relevant papers for CNV and SV approaches☆94Updated last year
- Ribo-seq TIS Hunter, predicting translation initiation sites and ORFs using riboseq data☆43Updated 3 months ago
- REDItools are python scripts to investigate RNA editing at genomic scale.☆69Updated 6 months ago
- R package designed to simplify structural variant analysis☆74Updated 4 years ago
- Variant Calling Pipeline Using GATK4 and Nextflow☆58Updated 2 years ago
- This WDL pipeline implements data pre-processing and initial variant calling according to the GATK Best Practices for germline SNP and In…☆55Updated 5 years ago
- Tip and tricks for BAM files☆86Updated 7 years ago
- A collection of resources to filter 'bad' probes from the Illumina 450k and EPIC methylation arrays☆30Updated 2 years ago
- ☆50Updated 4 years ago