» Articles » PMID: 23103880

The GEM Mapper: Fast, Accurate and Versatile Alignment by Filtration

Overview
Journal Nat Methods
Date 2012 Oct 30
PMID 23103880
Citations 272
Authors
Affiliations
Soon will be listed here.
Abstract

Because of ever-increasing throughput requirements of sequencing data, most existing short-read aligners have been designed to focus on speed at the expense of accuracy. The Genome Multitool (GEM) mapper can leverage string matching by filtration to search the alignment space more efficiently, simultaneously delivering precision (performing fully tunable exhaustive searches that return all existing matches, including gapped ones) and speed (being several times faster than comparable state-of-the-art tools).

Citing Articles

Germline structural variant as the cause of Lynch Syndrome in a family from Ecuador.

Llargues-Sistac G, Bonjoch L, Munoz J, Dominguez-Rovira X, Ocana T, Alvarez-Mora M NPJ Genom Med. 2025; 10(1):3.

PMID: 39821083 PMC: 11739559. DOI: 10.1038/s41525-025-00462-y.


GIN-TONIC: non-hierarchical full-text indexing for graph genomes.

Ozturk U, Mattavelli M, Ribeca P NAR Genom Bioinform. 2024; 6(4):lqae159.

PMID: 39664816 PMC: 11632618. DOI: 10.1093/nargab/lqae159.


Generative haplotype prediction outperforms statistical methods for small variant detection in next-generation sequencing data.

OFallon B, Bolia A, Durtschi J, Yang L, Fredrickson E, Best H Bioinformatics. 2024; 40(11).

PMID: 39298478 PMC: 11549014. DOI: 10.1093/bioinformatics/btae565.


A shift in chromatin binding of phosphorylated p38 precedes transcriptional changes upon oxidative stress.

Camilleri-Robles C, Climent-Canto P, Llorens-Giralt P, Klein C, Serras F, Corominas M FEBS Lett. 2024; 598(23):2926-2938.

PMID: 39218622 PMC: 11627000. DOI: 10.1002/1873-3468.15006.


Cell-type-specific loops linked to RNA polymerase II elongation in human neural differentiation.

Titus K, Simandi Z, Chandrashekar H, Paquet D, Phillips-Cremins J Cell Genom. 2024; 4(8):100606.

PMID: 38991604 PMC: 11406193. DOI: 10.1016/j.xgen.2024.100606.


References
1.
Hach F, Hormozdiari F, Alkan C, Hormozdiari F, Birol I, Eichler E . mrsFAST: a cache-oblivious algorithm for short-read mapping. Nat Methods. 2010; 7(8):576-7. PMC: 3115707. DOI: 10.1038/nmeth0810-576. View

2.
Langmead B, Trapnell C, Pop M, Salzberg S . Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol. 2009; 10(3):R25. PMC: 2690996. DOI: 10.1186/gb-2009-10-3-r25. View

3.
Li H, Durbin R . Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics. 2010; 26(5):589-95. PMC: 2828108. DOI: 10.1093/bioinformatics/btp698. View

4.
Karakoc E, Alkan C, ORoak B, Dennis M, Vives L, Mark K . Detection of structural variants and indels within exome data. Nat Methods. 2011; 9(2):176-8. PMC: 3269549. DOI: 10.1038/nmeth.1810. View

5.
Langmead B, Salzberg S . Fast gapped-read alignment with Bowtie 2. Nat Methods. 2012; 9(4):357-9. PMC: 3322381. DOI: 10.1038/nmeth.1923. View