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Uppsala University
- Uppsala, Sweden
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13:19
(UTC +01:00) - https://orcid.org/0000-0001-5235-6461
- https://orcid.org/0000-0001-5235-6461
Highlights
- Pro
Stars
Slides/notes and Jupyter notebook demos for an introductory course of numerical analysis/scientific computing
GeneMark-ETP: gene finding in eukaryotic genomes supported by transcriptome sequencing and protein homology
User-friendly Scheduler for sub-node tasks for HPC systems
Posit Cheat Sheets - Can also be found at https://posit.co/resources/cheatsheets/.
Collection of bioinformatics training materials
Adds SEQ and QUAL to secondary alignments from SAM/BAM/CRAM
Range-based for loops to iterate over a range of numbers or values
Reviews for the Journal of Open Source Software
NovoGraph: building whole genome graphs from long-read-based de novo assemblies
R-script for generating canonical diagrams of distributions to be used to describe Bayesian hierarchical models.
NextGenMap is a flexible highly sensitive short read mapping tool that handles much higher mismatch rates than comparable algorithms while still outperforming them in terms of runtime. This allows …
A program for the Maximum-likelihood analysis of population genomic data.
Standalone C library for assembling Illumina short reads in small regions
Embeddable genomic visualization component based on the Integrative Genomics Viewer
discoal is a coalescent simulation program capable of simulating models with recombination, selective sweeps, and demographic changes including population splits, admixture events, and ancient samples
MrBayes script used for the gene content analysis of Pisani et al. 2015
Scalable gVCF merging and joint variant calling for population sequencing projects