SciLifeLab / coursesLinks
Course homepages for some of the courses given at SciLifeLab
☆21Updated 6 years ago
Alternatives and similar repositories for courses
Users that are interested in courses are comparing it to the libraries listed below
Sorting:
- Nextflow RNA-Seq Best Practice analysis pipeline, used at the SciLifeLab National Genomics Infrastructure.☆51Updated 7 years ago
- An efficient way to guess the library type of your RNA-Seq data.☆32Updated 3 years ago
- An interactive web-tool for RNA-seq analysis☆70Updated last month
- A collection of scripts to assist in the retrieval of data from the ENA Browser☆93Updated 6 months ago
- ☆78Updated 11 years ago
- Issue tracker for the Biostar Handbook☆64Updated 3 years ago
- ☆63Updated 5 years ago
- 10x Genomics Linked-Read Diploid De Novo Assembler☆65Updated 7 years ago
- For biological deep sequencing data. Decompose a UCSC knownGenes/Ensembl GTF file into transcript regions (i.e. exons, introns, UTRs and…☆36Updated 2 years ago
- A catalogue of available long read sequencing data analysis tools☆85Updated last month
- A standalone interactive application for detecting biological significance on a set of genes☆40Updated 4 years ago
- Genomic Interactive Visualization Engine☆146Updated 3 years ago
- Materials for Spring 2018 Applied Genomics Course☆79Updated 7 years ago
- Building SuperTranscripts: A linear representation of transcriptome data☆68Updated 4 years ago
- List of IARC bioinformatics pipelines and resources☆56Updated 2 months ago
- Mapped QC analysis program☆43Updated 7 years ago
- Precision HLA typing from next-generation sequencing data☆78Updated this week
- materials for the RNA-Seq workshop on Trinity and Tuxedo, covering de novo and genome-guided transcript assembly and downstream analysis.☆48Updated 9 years ago
- Unsorted scripts for bioinformatics☆61Updated 4 years ago
- http://bioinformatics-core-shared-training.github.io/cruk-bioinf-sschool☆34Updated 10 years ago
- Software for predicting library complexity and genome coverage in high-throughput sequencing.☆94Updated last month
- My bioinfo toolbox☆50Updated last year
- ☆50Updated 4 years ago
- Demonstrating best practices for bioinformatics command line tools☆116Updated 5 years ago
- PrimerTree: Visually Assessing the Specificity and Informativeness of Primer Pairs☆52Updated 3 months ago
- Tip and tricks for BAM files☆86Updated 7 years ago
- BigWig and BAM utilities☆102Updated last year
- Maximum likelihood demultiplexing☆50Updated 11 months ago
- R package for inferring copy number from read depth☆32Updated 3 years ago
- Genomic data interpretation and visualization Workshop☆21Updated 2 months ago