michaelbarton / bioinformatics-career-surveyLinks
Survey of bioinformatics field
☆26Updated 13 years ago
Alternatives and similar repositories for bioinformatics-career-survey
Users that are interested in bioinformatics-career-survey are comparing it to the libraries listed below
Sorting:
- Modular blocks to build Snakemake workflows for reproducible NGS analyses☆22Updated 5 years ago
- Intro to workflows for efficient automated data analysis, using snakemake.☆32Updated 6 years ago
- Data Wrangling and Processing for Genomics☆72Updated last week
- BigWig manpulation tools using libBigWig and htslib☆29Updated last year
- Differential gene expression analysis and pathway analysis of RNAseq data☆32Updated last month
- fast webservices based query tool for large sets of genomic features☆25Updated 3 months ago
- A web based tool to manage and automate the processing of publicly available datasets.☆40Updated 4 years ago
- ☆10Updated 8 years ago
- deepStats: a stastitical toolbox for deeptools and genomic signals☆34Updated 4 years ago
- The command-line interface to GGD☆43Updated 2 years ago
- Allele frequency filter app☆14Updated 3 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- A python script used to annotate genomic intervals.☆18Updated 5 years ago
- ☆13Updated 7 years ago
- A Practical (And Opinionated) Guide To Analyzing 450K Data☆35Updated 10 years ago
- Fluff is a Python package that contains several scripts to produce pretty, publication-quality figures for next-generation sequencing exp…☆71Updated last year
- Exploration, clustering, visualization and classification of DNA damage patterns☆19Updated 4 years ago
- Tools for next-generation sequencing analysis☆89Updated 6 years ago
- Making Snakemake workflows into full-fledged command line tools since 1999.☆52Updated 7 years ago
- a set of NGS pipelines☆24Updated last week
- Easily run WDL workflows on GCP☆14Updated 3 years ago
- MetaSRA: normalized sample-specific metadata for the Sequence Read Archive☆44Updated last month
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- R package for Inference of differentially methylated regions (DMRs) from bisulfite sequencing☆61Updated 3 months ago
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago
- ☆35Updated 9 years ago
- Provides Quality Control of sequencing samples by deducing if there is batch effect and adjusts for it.☆35Updated 2 years ago
- create, manage, and upload track hubs for use in the UCSC genome browser☆54Updated last year
- This github repository contains code to reproduce the analysis in our paper "Variability in estimated gene expression among commonly used…☆28Updated last year
- A hierarchical multiscale model for inferring transcription factor binding from chromatin accessibility data.☆26Updated 9 years ago