Creating and using minimizer sketches in computational genomics
Processing large data sets has become an essential part of computational genomics.
Greatly increased availability of sequence data from multiple sources has fueled …
Greatly increased availability of sequence data from multiple sources has fueled …
MSV: a modular structural variant caller that reveals nested and complex rearrangements by unifying breakends inferred directly from reads
Structural variant (SV) calling belongs to the standard tools of modern bioinformatics for
identifying and describing alterations in genomes. Initially, this work presents several …
identifying and describing alterations in genomes. Initially, this work presents several …
Improving Performance of Multiple Sequence Alignment through Maximal Exact Match Identification
T Wehning - 2023 - essay.utwente.nl
Multiple sequence alignment is an integral part in the field of DNA analysis and genomics,
and it is necessary in order to properly identify evolutionary patterns as well as functional …
and it is necessary in order to properly identify evolutionary patterns as well as functional …
State-of-the-art structural variant calling: What went conceptually wrong and how to fix it?
Structural variant (SV) calling belongs to the standard tools of modern bioinformatics for
identifying and describing alterations in genomes. Initially, this work presents several …
identifying and describing alterations in genomes. Initially, this work presents several …