The availability of thousands of individual genomes of one species should boost rapid progress in personalized medicine or understanding of the interaction between genotype and phenotype, to name a few applications. A key operation useful in such analyses is aligning sequencing reads against a collection of genomes, which is costly with the use of existing algorithms due to their large memory requirements. We present MuGI, Multiple Genome Index, which reports all occurrences of a given pattern, in exact and approximate matching model, against a collection of thousand(s) genomes. Its unique feature is the small index size, which is customisable. It fits in a standard computer with 16-32 GB, or even 8 GB, of RAM, for the 1000GP collection of ...
Motivation: Alignment of similar whole genomes is often performed using anchors given by the Maximal...
International audience. Genomic and metagenomic fields, generating huge sets ofshort genomic sequenc...
Abstract. With the recent advances in DNA sequencing, it is now possible to have complete genomes of...
<div><p>The availability of thousands of individual genomes of one species should boost rapid progre...
The availability of thousands of individual genomes of one species should boost rapid progress in pe...
High-throughput sequencing (HTS) technologies have enabled rapid sequencing of genomes and large-sca...
Motivation: The search for exact matches of matches of substrings in pairs of large genomic sequence...
Searching for matches between large collections of short (14-30 nucleotides) words and sequence data...
The challenge of comparing two or more genomes that have undergone recombination and substantial amo...
Publisher Copyright: Copyright © 2021 Maarala et al.Computational pan-genomics utilizes information ...
The impending advent of population-scaled sequencing cohorts involving tens of millions of individua...
While short read aligners, which predominantly use the FM-index, are able to easily index one or a f...
Abstract Background The use of whole genome sequence has increased recently with rapid progression o...
Fast and robust algorithms and aligners have been developed to help the researchers in the analysis ...
Background: As the cost of DNA sequencing decreases, high-throughput sequencing technologies become ...
Motivation: Alignment of similar whole genomes is often performed using anchors given by the Maximal...
International audience. Genomic and metagenomic fields, generating huge sets ofshort genomic sequenc...
Abstract. With the recent advances in DNA sequencing, it is now possible to have complete genomes of...
<div><p>The availability of thousands of individual genomes of one species should boost rapid progre...
The availability of thousands of individual genomes of one species should boost rapid progress in pe...
High-throughput sequencing (HTS) technologies have enabled rapid sequencing of genomes and large-sca...
Motivation: The search for exact matches of matches of substrings in pairs of large genomic sequence...
Searching for matches between large collections of short (14-30 nucleotides) words and sequence data...
The challenge of comparing two or more genomes that have undergone recombination and substantial amo...
Publisher Copyright: Copyright © 2021 Maarala et al.Computational pan-genomics utilizes information ...
The impending advent of population-scaled sequencing cohorts involving tens of millions of individua...
While short read aligners, which predominantly use the FM-index, are able to easily index one or a f...
Abstract Background The use of whole genome sequence has increased recently with rapid progression o...
Fast and robust algorithms and aligners have been developed to help the researchers in the analysis ...
Background: As the cost of DNA sequencing decreases, high-throughput sequencing technologies become ...
Motivation: Alignment of similar whole genomes is often performed using anchors given by the Maximal...
International audience. Genomic and metagenomic fields, generating huge sets ofshort genomic sequenc...
Abstract. With the recent advances in DNA sequencing, it is now possible to have complete genomes of...