RCollins13 / HumanIdiogramLibraryLinks
Resource of human chromosome schematics & images
☆95Updated last year
Alternatives and similar repositories for HumanIdiogramLibrary
Users that are interested in HumanIdiogramLibrary are comparing it to the libraries listed below
Sorting:
- ☆78Updated 11 years ago
- Multi-sample somatic variant caller☆52Updated 3 years ago
- Very simple, pure python, BAM file reader☆79Updated 6 years ago
- ☆27Updated 4 months ago
- Scallop is a reference-based transcriptome assembler for RNA-seq☆91Updated 4 years ago
- JHU EN.600.649: Computational Genomics: Applied Comparative Genomics☆58Updated 7 years ago
- utilities for working with IGV: opening files remotely in either desktop IGV or a web viewer (igv.js), creating screenshots, etc.☆49Updated 6 years ago
- Nextflow RNA-Seq Best Practice analysis pipeline, used at the SciLifeLab National Genomics Infrastructure.☆51Updated 7 years ago
- Tools for next-generation sequencing analysis☆89Updated 6 years ago
- BigWig and BAM utilities☆98Updated last year
- Rapid Mapping-based Isoform Quantification from RNA-Seq Reads☆127Updated 3 years ago
- Galaxy RNA workbench☆40Updated 5 years ago
- List of IARC bioinformatics pipelines and resources☆53Updated this week
- ☆69Updated 3 years ago
- OLD REPOSITORY - Go to☆31Updated 7 years ago
- Contains the code from "Learning the Sequence Determinants of Alternative Splicing from Millions of Random Sequences"☆35Updated 9 years ago
- Bioconductor package "polyester", devel version. RNA-seq read simulator.☆94Updated 4 years ago
- Gene Fusion Visualiser☆51Updated 2 years ago
- SPP - R package for analysis of ChIP-seq and other functional sequencing data☆43Updated 4 years ago
- Tip and tricks for BAM files☆86Updated 7 years ago
- Materials for Spring 2018 Applied Genomics Course☆79Updated 6 years ago
- A combined strategy to identify circular RNAs (circRNAs and ciRNAs) (Zhang et al., Complementary Sequence-Mediated Exon Circularization, …☆61Updated 6 years ago
- Software for predicting library complexity and genome coverage in high-throughput sequencing.☆88Updated last year
- Genomic Interactive Visualization Engine☆145Updated 2 years ago
- ☆83Updated 3 years ago
- Battenberg algorithm and associated implementation script☆53Updated 5 years ago
- FireCloud Service Selector (FISS) -- Python bindings and CLI for FireCloud execution engine☆31Updated 7 months ago
- Snakemake-based workflow for detecting structural variants in genomic data☆80Updated 8 months ago
- Analysis of epigenetic signals captured by fragmentation patterns of cell-free DNA☆76Updated 5 years ago
- Relevant papers for CNV and SV approaches☆94Updated 11 months ago