Motivation: Seed filtering is critical in DNA read mapping, a process where billions of DNA fragments (reads) sampled from a donor are mapped onto a reference genome to identify …
J Kim, D Senol, H Xin, D Lee, M Alser… - Pacific Symp …, 2017 - people.inf.ethz.ch
In the past couple of decades, high-throughput sequencing (HTS) technology has resulted in a massive influx of available genetic data. Using HTS technology, genomes are sequenced …
C Golden, D Ilan, N Cebry, C Batten - arXiv preprint arXiv:2401.11685, 2024 - arxiv.org
DNA sequence alignment is an important workload in computational genomics. Reference- guided DNA assembly involves aligning many read sequences against candidate locations …
Sequence alignment is a fundamental operation in genomic analysis where DNA fragments called reads are mapped to a long reference DNA sequence. There exist a number of (in) …
Read mapping is currently the performance bottleneck of genome sequence analysis since it needs to perform costly approximate string matching to identify the potential matches …
We present Masai, a read mapper representing the state-of-the-art in terms of speed and accuracy. Our tool is an order of magnitude faster than RazerS 3 and mrFAST, 2–4 times …
Advancements in sequencing technology have brought a large increase in the quantity of raw sequencing data. To cope with the ever growing sequence data sets, efficient read …
DNA read mapping is a ubiquitous task in bioinformatics, and many tools have been developed to solve the read mapping problem. However, there are two trends that are …
Motivation High throughput DNA sequencing (HTS) technologies generate an excessive number of small DNA segments-called short reads-that cause significant computational …