fedeoliv / Rosalind-Problems
Bioinformatics Algorithms
☆15Updated 11 years ago
Alternatives and similar repositories for Rosalind-Problems:
Users that are interested in Rosalind-Problems are comparing it to the libraries listed below
- Solutions to problems from http://rosalind.info/☆36Updated 12 years ago
- Rosalind Bioinformatics Problems☆31Updated 9 years ago
- Workshop content for http://dib-training.readthedocs.org/en/pub/2016-01-13-adv-beg-shell.html☆12Updated 6 years ago
- repository for the code featured in the blog☆22Updated 16 years ago
- CRUK Bioinformatics Workshop September 2017☆18Updated 7 years ago
- ATAC-seq lab for BIOINF525☆10Updated 8 years ago
- Little sequence file utilities meant to work within Unix pipelines☆37Updated 10 years ago
- ☆45Updated 7 years ago
- All kinds of NGS analysis pipeline☆12Updated 5 years ago
- Methods to integrate data from multiple genome sequencing datasets and form consensus variant calls☆43Updated 3 years ago
- Miscellaneous Bioinformatics scripts etc mostly in Python☆45Updated 2 weeks ago
- ☆51Updated 5 years ago
- A hierarchical multiscale model for inferring transcription factor binding from chromatin accessibility data.☆26Updated 8 years ago
- High-performance error correction for Illumina resequencing data☆69Updated 8 years ago
- chia pet analysis software☆25Updated 6 years ago
- A repository for my solutions to problems from - http://www.rosalind.info☆21Updated 3 years ago
- Readme☆10Updated 4 years ago
- RNA-Sequencing data differential expression analysis pipeline. Performs: genome coverage (via bedtools and HTSeq), generates Circos code …☆55Updated 12 years ago
- Bring Your Own Bioinformatics☆27Updated 8 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆55Updated 7 years ago
- A toolkit for working with ATAC-seq data.☆24Updated 8 months ago
- ☆22Updated 4 years ago
- Published methods☆15Updated 8 years ago
- Tools for next-generation sequencing analysis☆88Updated 5 years ago
- NGS DNA best practice pipeline for Illumina sequencing - alignment, variant calling, annotation and QC☆16Updated 9 months ago
- Analysis from kallisto paper☆32Updated 9 years ago
- Bioinformatics scripts☆13Updated last month
- ☆15Updated 2 years ago
- Explore, compare, and evaluate Bioconductor packages related to genomic copy number analysis☆21Updated last year
- ThermoAlign: software for automated primer design☆25Updated 6 years ago