Limitation of number of strains and persistence of false positive loci in QTL mapping using recombinant inbred strains.

While the identification of causal genes of quantitative trait loci (QTL) remains a difficult problem in the post-genome era, the number of QTL continues to accumulate, mainly identified using the recombinant inbred (RI) strains. Over the last decade, hundreds of publications have reported nearly a...

Full description

Bibliographic Details
Main Authors: Lishi Wang, Yan Jiao, Yanhong Cao, Gaifen Liu, Yongjun Wang, Weikuan Gu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4102522?pdf=render
id doaj-e82bb6097ab64d229947a10f537f68ca
record_format Article
spelling doaj-e82bb6097ab64d229947a10f537f68ca2020-11-25T01:58:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0197e10230710.1371/journal.pone.0102307Limitation of number of strains and persistence of false positive loci in QTL mapping using recombinant inbred strains.Lishi WangYan JiaoYanhong CaoGaifen LiuYongjun WangWeikuan GuWhile the identification of causal genes of quantitative trait loci (QTL) remains a difficult problem in the post-genome era, the number of QTL continues to accumulate, mainly identified using the recombinant inbred (RI) strains. Over the last decade, hundreds of publications have reported nearly a thousand QTL identified from RI strains. We hypothesized that the inaccuracy of most of these QTL makes it difficult to identify causal genes. Using data from RI strains derived from C57BL/6J (B6) X DBA/2J (D2), we tested the possibility of detection of reliable QTL with different numbers of strains in the same trait in five different traits. Our results indicated that studies using RI strains of less than 30 in general have a higher probability of failing to detect reliable QTL. Errors in many studies could include false positive loci, switches between QTL with small and major effects, and missing the real major loci. The similar data was obtained from a RI strain population derived from a different pair of parents and a RI strain population of rat. Thus, thousands of reported QTL from studies of RI strains may need to be double-checked for accuracy before proceeding to causal gene identification.http://europepmc.org/articles/PMC4102522?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Lishi Wang
Yan Jiao
Yanhong Cao
Gaifen Liu
Yongjun Wang
Weikuan Gu
spellingShingle Lishi Wang
Yan Jiao
Yanhong Cao
Gaifen Liu
Yongjun Wang
Weikuan Gu
Limitation of number of strains and persistence of false positive loci in QTL mapping using recombinant inbred strains.
PLoS ONE
author_facet Lishi Wang
Yan Jiao
Yanhong Cao
Gaifen Liu
Yongjun Wang
Weikuan Gu
author_sort Lishi Wang
title Limitation of number of strains and persistence of false positive loci in QTL mapping using recombinant inbred strains.
title_short Limitation of number of strains and persistence of false positive loci in QTL mapping using recombinant inbred strains.
title_full Limitation of number of strains and persistence of false positive loci in QTL mapping using recombinant inbred strains.
title_fullStr Limitation of number of strains and persistence of false positive loci in QTL mapping using recombinant inbred strains.
title_full_unstemmed Limitation of number of strains and persistence of false positive loci in QTL mapping using recombinant inbred strains.
title_sort limitation of number of strains and persistence of false positive loci in qtl mapping using recombinant inbred strains.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description While the identification of causal genes of quantitative trait loci (QTL) remains a difficult problem in the post-genome era, the number of QTL continues to accumulate, mainly identified using the recombinant inbred (RI) strains. Over the last decade, hundreds of publications have reported nearly a thousand QTL identified from RI strains. We hypothesized that the inaccuracy of most of these QTL makes it difficult to identify causal genes. Using data from RI strains derived from C57BL/6J (B6) X DBA/2J (D2), we tested the possibility of detection of reliable QTL with different numbers of strains in the same trait in five different traits. Our results indicated that studies using RI strains of less than 30 in general have a higher probability of failing to detect reliable QTL. Errors in many studies could include false positive loci, switches between QTL with small and major effects, and missing the real major loci. The similar data was obtained from a RI strain population derived from a different pair of parents and a RI strain population of rat. Thus, thousands of reported QTL from studies of RI strains may need to be double-checked for accuracy before proceeding to causal gene identification.
url http://europepmc.org/articles/PMC4102522?pdf=render
work_keys_str_mv AT lishiwang limitationofnumberofstrainsandpersistenceoffalsepositivelociinqtlmappingusingrecombinantinbredstrains
AT yanjiao limitationofnumberofstrainsandpersistenceoffalsepositivelociinqtlmappingusingrecombinantinbredstrains
AT yanhongcao limitationofnumberofstrainsandpersistenceoffalsepositivelociinqtlmappingusingrecombinantinbredstrains
AT gaifenliu limitationofnumberofstrainsandpersistenceoffalsepositivelociinqtlmappingusingrecombinantinbredstrains
AT yongjunwang limitationofnumberofstrainsandpersistenceoffalsepositivelociinqtlmappingusingrecombinantinbredstrains
AT weikuangu limitationofnumberofstrainsandpersistenceoffalsepositivelociinqtlmappingusingrecombinantinbredstrains
_version_ 1724967050550444032