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Cited by 241

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

AlienTrimmer: A tool to quickly and accurately trim off multiple short contaminant sequences from high-throughput sequencing reads

Open access
Criscuolo, Alexis, Brisse, Sylvain·2013·Genomics

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Citations

Cites

Show all 4 references

Research works printed but not linked: 14

  1. Lindgreen, 2012, AdapterRemoval: easy cleaning of next-generation sequencing reads, BMC Res. Notes, 5, 337, 10.1186/1756-0500-5-337 · DOI · Paper page
  2. Dodt, 2012, FLEXBAR—flexible barcode and adapter processing for next-generation sequencing platforms, Biology, 1, 895, 10.3390/biology1030895 · DOI · Paper page
  3. Kong, 2011, Btrim: a fast, lightweight adapter and quality trimming program for next-generation sequencing technologies, Genomics, 98, 152, 10.1016/j.ygeno.2011.05.009 · DOI · Paper page
  4. Li, 2009, Fast and accurate short read alignment with Burrows–Wheeler transform, Bioinformatics, 25, 1754, 10.1093/bioinformatics/btp324 · DOI · Paper page
  5. Li, 2009, The sequence alignment/map (SAM) format and SAMtools, Bioinformatics, 25, 2078, 10.1093/bioinformatics/btp352 · DOI · Paper page
  6. Miller, 2010, Assembly algorithms for next-generation sequencing data, Genomics, 95, 315, 10.1016/j.ygeno.2010.03.001 · DOI · Paper page
  7. Swets, 2000, Better decision through science, Sci. Am., 283, 82, 10.1038/scientificamerican1000-82 · DOI · Paper page
  8. Hanley, 1982, The meaning and use of the area under a receiver operating characteristic (ROC) curve, Radiology, 143, 29, 10.1148/radiology.143.1.7063747 · DOI · Paper page
  9. Nakamura, 2011, Sequence-specific error profile of Illumina sequencers, Nucleic Acids Res., 39, e90, 10.1093/nar/gkr344 · DOI · Paper page
  10. Smeds, 2011, ConDeTri — a content dependent read trimmer for Illumina data, PLoS One, 6, e26314, 10.1371/journal.pone.0026314 · DOI · Paper page
  11. Minoche, 2011, Evaluation of genomic high-throughput sequencing data generated on Illumina HiSeq and Genome Analyzer systems, Genome Biol., 12, R112, 10.1186/gb-2011-12-11-r112 · DOI · Paper page
  12. Yu, 2012, How do alignment programs perform on sequencing data with varying qualities and from repetitive regions?, BioData Min., 5, 6, 10.1186/1756-0381-5-6 · DOI
  13. Cock, 2009, The Sanger FASTQ file format for sequences with quality scores, and the Solexa/Illumina FASTQ variants, Nucleic Acids Res., 38, 1767, 10.1093/nar/gkp1137 · DOI · Paper page
  14. Knuth, 1973, vol. 3

Cited by

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Metadata

Authors
Criscuolo, A., & Brisse, S.
Venue
Genomics
Publisher
Elsevier BV
Published
2013-11
Volume
102
Issue
5-6
Pages
500-506
ISSN
0888-7543 (ISSN-L)
OpenAlex
W2007703905
Cited by
241
References
4
FWCI
2.82
Type
journal article
Language
en
Open access
bronze
Licence
Funders
Région Ile-de-France

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CoChat. (2026). Citation check: AlienTrimmer: A tool to quickly and accurately trim off multiple short contaminant sequences from high-throughput sequencing reads. https://app.cochat.ai/papers/10.1016/j.ygeno.2013.07.011
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Criscuolo, A., & Brisse, S. (2013). AlienTrimmer: A tool to quickly and accurately trim off multiple short contaminant sequences from high-throughput sequencing reads. Genomics. https://doi.org/10.1016/j.ygeno.2013.07.011

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.