TAP: a targeted clinical genomics pipeline for detecting transcript variants using RNA-seq data.

Chiu R, Nip KM, Chu J, Birol I

DOI: 10.1186/s12920-018-0402-6
Published: 2018 Sep 10
Container: BMC medical genomics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1186/s12920-018-0402-6,
  title = {TAP: a targeted clinical genomics pipeline for detecting transcript variants using RNA-seq data.},
  author = {Chiu R and Nip KM and Chu J and Birol I},
  year = {2018},
  journal = {BMC medical genomics},
  doi = {10.1186/s12920-018-0402-6},
  url = {https://doi.org/10.1186/s12920-018-0402-6}
}

RIS

TY  - JOUR
TI  - TAP: a targeted clinical genomics pipeline for detecting transcript variants using RNA-seq data.
AU  - Chiu R
AU  - Nip KM
AU  - Chu J
AU  - Birol I
PY  - 2018
JO  - BMC medical genomics
DO  - 10.1186/s12920-018-0402-6
UR  - https://doi.org/10.1186/s12920-018-0402-6
ER  -

APA

R, C., KM, N., J, C., & I, B. (2018). TAP: a targeted clinical genomics pipeline for detecting transcript variants using RNA-seq data.. BMC medical genomics. https://doi.org/10.1186/s12920-018-0402-6

Source records

pubmed · retrieved 2026-09-26T03:56:31.590Z