Flype: Software for enabling personalized medicine.
Flype: Software for enabling personalized medicine.
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Flype:用于启用个性化医学的软件。
DOI:
10.1002/ajmg.c.31867
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发表时间:
2021-03
期刊:
影响因子:
--
通讯作者:
Khandekar JD
中科院分区:
文献类型:
--
作者:
Helseth DL Jr;Gulukota K;Miller N;Yang M;Werth T;Sabatini LM;Bouma M;Dunnenberger HM;Wake DT;Hulick PJ;Kaul KL;Khandekar JD
The advent of next generation DNA sequencing (NGS) has revolutionized clinical medicine by enabling wide‐spread testing for genomic anomalies and polymorphisms. With that explosion in testing, however, come several informatics challenges including managing large amounts of data, interpreting the results and providing clinical decision support. We present Flype, a web‐based bioinformatics platform built by a small group of bioinformaticians working in a community hospital setting, to address these challenges by allowing us to: (a) securely accept data from a variety of sources, (b) send orders to a variety of destinations, (c) perform secondary analysis and annotation of NGS data, (d) provide a central repository for all genomic variants, (e) assist with tertiary analysis and clinical interpretation, (f) send signed out data to our EHR as both PDF and discrete data elements, (g) allow population frequency analysis and (h) update variant annotation when literature knowledge evolves. We discuss the multiple use cases Flype supports such as (a) in‐house NGS tests, (b) in‐house pharmacogenomics (PGX) tests, (c) dramatic scale‐up of genomic testing using an external lab, (d) consumer genomics using two external partners, and (e) a variety of reporting tools. The source code for Flype is available upon request to the authors.
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