GATES: A Lightweight Tool Automating Pathogenic Variant Discovery From Raw Whole-Exome Sequencing Data.

Bambach NE, Ricarte-Filho JC, Reichenberger ER, Franco AT

Open source

DOI: 10.1177/11769351261485924
Published: 2026
Container: Cancer informatics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1177/11769351261485924,
  title = {GATES: A Lightweight Tool Automating Pathogenic Variant Discovery From Raw Whole-Exome Sequencing Data.},
  author = {Bambach NE and Ricarte-Filho JC and Reichenberger ER and Franco AT},
  year = {2026},
  journal = {Cancer informatics},
  doi = {10.1177/11769351261485924},
  url = {https://doi.org/10.1177/11769351261485924}
}

RIS

TY  - JOUR
TI  - GATES: A Lightweight Tool Automating Pathogenic Variant Discovery From Raw Whole-Exome Sequencing Data.
AU  - Bambach NE
AU  - Ricarte-Filho JC
AU  - Reichenberger ER
AU  - Franco AT
PY  - 2026
JO  - Cancer informatics
DO  - 10.1177/11769351261485924
UR  - https://doi.org/10.1177/11769351261485924
ER  -

APA

NE, B., JC, R., ER, R., & AT, F. (2026). GATES: A Lightweight Tool Automating Pathogenic Variant Discovery From Raw Whole-Exome Sequencing Data.. Cancer informatics. https://doi.org/10.1177/11769351261485924

Source records

pubmed · retrieved 2026-11-10T12:09:23.675Z
europe-pmc · retrieved 2026-11-10T12:09:23.733Z
doaj · retrieved 2026-11-10T12:09:23.674Z