Marker density and read depth for genotyping populations using genotyping-by-sequencing.
Marker density and read depth for genotyping populations using genotyping-by-sequencing.
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DOI:
10.1534/genetics.112.147710
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发表时间:
2013-04
期刊:
影响因子:
3.3
通讯作者:
de Leon N
中科院分区:
文献类型:
--
作者:
Beissinger TM;Hirsch CN;Sekhon RS;Foerster JM;Johnson JM;Muttoni G;Vaillancourt B;Buell CR;Kaeppler SM;de Leon N
Genotyping-by-sequencing (GBS) approaches provide low-cost, high-density genotype information. However, GBS has unique technical considerations, including a substantial amount of missing data and a nonuniform distribution of sequence reads. The goal of this study was to characterize technical variation using this method and to develop methods to optimize read depth to obtain desired marker coverage. To empirically assess the distribution of fragments produced using GBS, ∼8.69 Gb of GBS data were generated on the Zea mays reference inbred B73, utilizing ApeKI for genome reduction and single-end reads between 75 and 81 bp in length. We observed wide variation in sequence coverage across sites. Approximately 76% of potentially observable cut site-adjacent sequence fragments had no sequencing reads whereas a portion had substantially greater read depth than expected, up to 2369 times the expected mean. The methods described in this article facilitate determination of sequencing depth in the context of empirically defined read depth to achieve desired marker density for genetic mapping studies.
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影响因子:
3.7
作者:
Baird NA;Etter PD;Atwood TS;Currey MC;Shiver AL;Lewis ZA;Selker EU;Cresko WA;Johnson EA
通讯作者:
Johnson EA
影响因子:
3.7
作者:
Baxter SW;Davey JW;Johnston JS;Shelton AM;Heckel DG;Jiggins CD;Blaxter ML
通讯作者:
Blaxter ML
影响因子:
64.8
作者:
通讯作者:
--
影响因子:
4.4
作者:
Chutimanitsakun Y;Nipper RW;Cuesta-Marcos A;Cistué L;Corey A;Filichkina T;Johnson EA;Hayes PM
通讯作者:
Hayes PM
影响因子:
3.3
作者:
Lough, Ashley N.;Roark, Leah M.;Newton, Kathleen J.
通讯作者:
Newton, Kathleen J.