5 posts tagged with bioinformatics by grouse.
Displaying 1 through 5 of 5.

Acidbio

Our new verification system, which tests for correct behavior in bioinformatics software packages. We crafted tests to unify correct behavior when tools encounter various edge cases—potentially unexpected inputs that exemplify the limits of the format. Inspired by the web standards Acid tests.
posted by grouse on May 23, 2022 - 2 comments

Polyidus: identifying viral integration sites from chimeric sequencing reads

The free Polyidus software identifies the exact genomic regions for integration of a known virus. We developed Polyidus to identify viral integration sites with chimeric sequencing reads from any paired-end sequencing data. First, Polyidus aligns reads to a viral genome. It allows for partial mapping using local alignment, and removes any sequencing fragment where neither read maps to the virus. Second, Polyidus aligns the selected reads to the host genome, permitting partial mapping. Third, Polyidus identifies chimeric reads: those reads mapped partially to the host genome and partially to the virus genome. Fourth, for each chimeric read, Polyidus reports the start and strand of integration in both the host and viral genomes. Polyidus also reports the number of chimeric reads supporting each integration site. [more inside]
posted by grouse on Apr 13, 2022 - 0 comments

peaKO

We have created a new method to find transcription factor motifs in ChIP-seq data using knockout controls. Available on PyPI and GitHub.
posted by grouse on May 5, 2021 - 0 comments

Virtual ChIP-seq

Our new method predicts transcription factor and chromatin factor locations in a cell type using new kinds of data like chromatin factor binding in other cell types and learning the association of gene expression patterns with chromatin factor binding patterns. We've made free software available and a track hub that can load our predictions for 36 chromatin factors in 33 human tissue types into the UCSC Genome Browser.
posted by grouse on Feb 17, 2019 - 1 comment

Umap and Bismap: quantifying genome and methylome mappability

Many biological experiments use DNA sequencing as a readout. We can often map the sequenced DNA back to a specific region of the genome. Sometimes, however, we can't. Genomic data is less reliable in those regions. My lab has developed software that makes it easy to identify these regions. We also developed a new method that lets us find those regions in the context of bisulfite sequencing, a technique used to determine where DNA is chemically modified. [more inside]
posted by grouse on Dec 20, 2016 - 0 comments

Page: 1