BUStools / BUS-formatLinks
BUS format specification
☆13Updated 6 years ago
Alternatives and similar repositories for BUS-format
Users that are interested in BUS-format are comparing it to the libraries listed below
Sorting:
- ProSolo, variant calling from single cell DNA-seq data, or: bulk backing vocals for single cell solos.☆21Updated 4 years ago
- Improved multi-sample transcript abundance estimates using adaptive priors☆20Updated 7 years ago
- ☆21Updated 11 months ago
- R Interface to the NCBI SRA metadata☆23Updated 7 years ago
- A program for fast and accurate genome-guided transcripts reconstruction and quantification from RNA-seq (Supporting Pacbio single-end)☆24Updated 4 years ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- Tools for working FASTQ files from sequencers (R1/R2/I1/I2)☆12Updated 11 months ago
- FREE Divergence Error-Correcting DNA Barcodes☆10Updated 7 years ago
- Calib clusters barcode tagged paired-end reads based on their barcode and sequence similarity.☆39Updated 2 years ago
- A (very) fast program for getting statistics about a fastq file, the way I need them, written in Rust☆31Updated last week
- Bedfile perturbation tool☆17Updated last month
- Callable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer☆21Updated 4 years ago
- Somatic (mosaic) SNV caller for 10X Genomics data using random forest classification and feature-based filters☆23Updated 6 years ago
- BED QC tool (in the making)☆16Updated 3 years ago
- Calculate and plot distributions of genomic ranges☆26Updated 7 months ago
- A Rust library for storing generic genomic data by sorted chromosome name☆17Updated last year
- Slinker offers a succinct and complementary method to visualise RNA-Seq data through superTranscripts.☆19Updated 3 years ago
- Bam Read Index - Extract alignments from a bam file by readname☆28Updated last year
- Rapid and robust analysis of RNA-Seq experiments.☆32Updated 9 years ago
- Chromatin segmentation in R☆19Updated 7 years ago
- Visualization tool for temporal clonal evolution.☆18Updated 5 years ago
- Allele-Specific Quantification of Structural Variations in Cancer Genomes☆18Updated 6 years ago
- Teaching modules for Human Genome Variation Lab.☆20Updated 5 months ago
- Comprehensive Human Expressed SequenceS☆18Updated 4 months ago
- Unfazed by genomic variant phasing☆27Updated last year
- BigWig manpulation tools using libBigWig and htslib☆29Updated last year
- Accurate, Lightweight Clustering of de novo Transcriptomes using Fragment Equivalence Classes☆31Updated last year
- ☆11Updated 2 years ago
- ☆14Updated 2 months ago
- ☆13Updated 5 years ago