chess-genome / chessView external linksLinks
Comprehensive Human Expressed SequenceS
☆19Jul 13, 2025Updated 7 months ago
Alternatives and similar repositories for chess
Users that are interested in chess are comparing it to the libraries listed below
Sorting:
- ☆69Feb 5, 2026Updated last week
- IsoVis enables fast and informative visualization of isoform structures and expression levels.☆13Feb 5, 2026Updated last week
- Bioconductor package that makes BIG data pint-sized.☆21Feb 12, 2024Updated 2 years ago
- ProphAsm – a rapid computation of simplitigs directly from k-mer sets☆25Feb 17, 2023Updated 2 years ago
- Haplotype-based somatic genome simulator☆10May 19, 2017Updated 8 years ago
- Finding cryptic relationships to boost disease gene detection☆12May 31, 2023Updated 2 years ago
- SeqOthello supports fast coverage query and containment query.☆12May 8, 2019Updated 6 years ago
- Isoform-level expression patterns in single-cell RNA-sequencing data☆11Apr 20, 2023Updated 2 years ago
- k-mer probability logo☆11Jan 20, 2023Updated 3 years ago
- ☆11May 3, 2022Updated 3 years ago
- Community effort to evaluate computational methods for the detection and quantification of poly(A) sites and estimating their differentia…☆14Jan 11, 2024Updated 2 years ago
- SODAR: System for Omics Data Access and Retrieval☆19Feb 6, 2026Updated last week
- R package for gene selection using k-NN graphs.☆13Jun 12, 2023Updated 2 years ago
- Spark VCF data source implementation for Dataframes☆15Jul 15, 2022Updated 3 years ago
- List of conferences with talk videos posted online☆12Sep 23, 2023Updated 2 years ago
- Polygenic score calculation from VCF in Nim.☆15Nov 22, 2020Updated 5 years ago
- The shiny app that accompanies the ngsReports R package☆13Jun 10, 2021Updated 4 years ago
- Repository with all my container recipes 👩🍳☆17Sep 9, 2024Updated last year
- Build single sample pair-based (rule-based) classifiers using top-score pairs or random forest for multi-class problems.☆13May 1, 2023Updated 2 years ago
- Ultra-efficient and sensitive method to search for Open Reading Frames in spliced genomes guided by reference annotation to maximize prot…☆43Dec 30, 2025Updated last month
- Generate and process BAM files from Illumina sequencing instrument files☆23Feb 25, 2016Updated 9 years ago
- ORF Quantification pipeline for Alternative Splicing☆16May 11, 2021Updated 4 years ago
- ☆22Feb 5, 2025Updated last year
- Long RNA-seq analysis workflow☆21Oct 13, 2025Updated 4 months ago
- Search for activating regulatory variants in the tumor genome☆14Apr 11, 2025Updated 10 months ago
- ☆24Updated this week
- ☆14Dec 13, 2023Updated 2 years ago
- DeepMosaic is a deep-learning-based mosaic single nucleotide classification tool without the need of matched control information.☆49Dec 6, 2025Updated 2 months ago
- Library for indexing VCF files for random access searches by rsID☆17Feb 2, 2026Updated last week
- ☆24Jul 28, 2016Updated 9 years ago
- PRS-on-SPARK☆18Feb 4, 2021Updated 5 years ago
- Prediction of mRNA subcellular localization using deep recurrent neural networks☆15Jul 19, 2019Updated 6 years ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Apr 7, 2022Updated 3 years ago
- ☆26Oct 8, 2025Updated 4 months ago
- k-mer similarity analysis pipeline☆22Nov 20, 2025Updated 2 months ago
- Mapping-free software for fishing relevant reads in an RNA-Seq sample☆19Dec 9, 2020Updated 5 years ago
- Enjoy your transcriptomic data and analysis responsibly - like sipping a cocktail☆81Jan 22, 2026Updated 3 weeks ago
- Scalable inference of gene regulatory networks using Apache Spark and XGBoost☆20Feb 8, 2018Updated 8 years ago
- Rapid and accurate ancestry inference using SNVs.☆28Aug 15, 2025Updated 5 months ago