googlegenomics / getting-started-bigquery
Examples of how to get started with genomics data in BigQuery in many languages.
☆53Updated 7 years ago
Alternatives and similar repositories for getting-started-bigquery:
Users that are interested in getting-started-bigquery are comparing it to the libraries listed below
- Advanced BigQuery examples on genomic data.☆89Updated 7 years ago
- Quality control methods for human genomic variants.☆62Updated 2 years ago
- Documentation for the Google Genomics cookbook.☆142Updated 4 years ago
- Provides access to complex Bioinformatics software (even BioLinux!) in just one command.☆76Updated 7 years ago
- A scalable genome browser. Apache 2 licensed.☆125Updated 2 years ago
- Example Cloud Datalab iPython Notebooks for genomics use cases.☆25Updated 7 years ago
- Server wrapper that turns command line tools into web services☆61Updated 6 years ago
- Deprecated : Use https://github.com/drpowell/degust☆44Updated 7 years ago
- Analysis of the penetrance of missense variants and tolerability of loss-of-function variants in PRNP☆9Updated 8 years ago
- [Historical] Reproducible Analyses for Bioinformatics☆106Updated 6 years ago
- Lesson on data analysis and visualization in R for genomics☆42Updated 6 years ago
- Snakemake library for bioinformatics programs, with a focus on next-generation sequencing☆22Updated 9 years ago
- Horizon chart js library for DNA data.☆61Updated 8 years ago
- Genome Annotation for the Masses☆36Updated 7 years ago
- Metadata database for ENCODE project☆112Updated last month
- SVG based genome viewer written in javascript using D3☆33Updated 9 years ago
- Interactive web-based genome browser.☆227Updated 5 years ago
- conda recipes for genomic data☆85Updated 3 years ago
- Request for comments on interchangeable bioinformatics containers☆40Updated 5 years ago
- Translation layer between the GDC Data Dictionary and psqlgraph☆28Updated last year
- Streaming fragment assignment and quantification for high-throughput sequencing.☆35Updated 5 years ago
- Analysis examples based on the ISB-CGC hosted TCGA data, using Python and IPython Notebooks.☆54Updated 5 years ago
- A fast Python library for VCF files leveraging Cython for speed.☆52Updated 7 years ago
- EDGE is a highly adaptable bioinformatics platform that allows laboratories to quickly analyze and interpret genomic sequence data.☆73Updated last month
- A R/shiny web application to browse and compare public RNA-seq / ChIP-seq / CAGE datasets☆18Updated 4 years ago
- Chart to aid in understanding mutations and their location on a gene.☆22Updated 2 years ago
- Scalable RNA-seq analysis☆73Updated 4 years ago
- Interactive Visual Analysis of differential gene expression test results☆22Updated 8 years ago
- Rapid Mapping-based Isoform Quantification from RNA-Seq Reads☆126Updated 2 years ago
- paplot creates various dynamic and interactive reports for cancer genome analysis.☆25Updated 2 years ago