Evidence map›Paper›PMID 24713734›Full record

ArticleAmerican journal of clinical pathology2014

BRAF pyrosequencing analysis aided by a lookup table.

Matthew T Olson, Colleen Harrington, Katie Beierl, Guoli Chen, Michele Thiess, Alan O'Neill, Janis M Taube, Martha A Zeiger, Ming-Tseh Lin, James R Eshleman

Abstract read
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Article in American journal of clinical pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Matthew T OlsonThe Sol Goldman Pancreatic Cancer Research Center, Professor of Pathology and Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD 21231; jeshlema@jhmi.edu.
Colleen Harrington
Katie Beierl
Guoli Chen
Michele Thiess
Alan O'Neill
Janis M Taube
Martha A Zeiger
Ming-Tseh Lin
James R Eshleman

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
NCI NIH HHS P30 CA006973
6 · The paper itself

Abstract

objectivesBRAF mutations have substantial therapeutic, diagnostic, and prognostic significance, so detecting and specifying them is an important part of the workload of molecular pathology laboratories. Pyrosequencing assays are well suited for this analysis but can produce complex results. Therefore, we introduce a pyrosequencing lookup table based on Pyromaker that assists the user in generating hypotheses for solving complex pyrosequencing results.

methodsThe lookup table contains all known mutations in the sequenced region and the positions in the dispensation sequence at which changes would occur with those mutations. We demonstrate the lookup table using a homebrew dispensation sequence for BRAF codons 596 to 605 as well as a commercially available kit-based dispensation sequence for codons 599 to 600.

resultsThese results demonstrate that the homebrew dispensation sequence unambiguously identifies all known BRAF mutations in this region, whereas the kit-based dispensation sequence has one unresolvable degeneracy that could be solved with the addition of two injections.

conclusionsUsing the lookup table and confirmatory virtual pyrogram, we unambiguously solved clinical pyrograms of the complex mutations V600K (c.1798_1799delGTinsAA), V600R (c.1798_1799delGTinsAG), V600D (c.1799_1800delTGinsAT), V600E (c.1799_1800delTGinsAA), and V600_K601delinsE (c.1799_1801delTGA). In addition, we used the approach to hypothesize and confirm a new mutation in human melanoma, V600_K601delinsEI (c.1799_1802delTGAAinsAAAT).

Indexed as

Genetic Predisposition to DiseaseGenetic TestingHumansMelanomaMutationPathology, MolecularProto-Oncogene Proteins B-rafSequence Analysis, DNASkin NeoplasmsProto-Oncogene Proteins B-rafBioinformaticsBRAF mutationsPyromakerPyrosequencingPyrosequencing analysis

Identifiers

PMID24713734
PMCPMC4643461

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.