Standard
Estimation of allele frequency and association mapping using next-generation sequencing data. / Kim, Su Yeon; Lohmueller, Kirk E; Albrechtsen, Anders; Li, Yingrui; Korneliussen, Thorfinn Sand; Tian, Geng; Grarup, Niels; Jiang, Tao; Andersen, Gitte; Witte, Daniel; Jorgensen, Torben; Hansen, Torben; Pedersen, Oluf; Wang, Jun; Nielsen, Rasmus.
I:
B M C Bioinformatics, Bind 12, 2011, s. 231.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
Kim, SY, Lohmueller, KE
, Albrechtsen, A, Li, Y
, Korneliussen, TS, Tian, G
, Grarup, N, Jiang, T, Andersen, G, Witte, D, Jorgensen, T
, Hansen, T, Pedersen, O, Wang, J
& Nielsen, R 2011, '
Estimation of allele frequency and association mapping using next-generation sequencing data',
B M C Bioinformatics, bind 12, s. 231.
https://doi.org/10.1186/1471-2105-12-231APA
Kim, S. Y., Lohmueller, K. E.
, Albrechtsen, A., Li, Y.
, Korneliussen, T. S., Tian, G.
, Grarup, N., Jiang, T., Andersen, G., Witte, D., Jorgensen, T.
, Hansen, T., Pedersen, O., Wang, J.
, & Nielsen, R. (2011).
Estimation of allele frequency and association mapping using next-generation sequencing data.
B M C Bioinformatics,
12, 231.
https://doi.org/10.1186/1471-2105-12-231Vancouver
Kim SY, Lohmueller KE
, Albrechtsen A, Li Y
, Korneliussen TS, Tian G o.a.
Estimation of allele frequency and association mapping using next-generation sequencing data.
B M C Bioinformatics. 2011;12:231.
https://doi.org/10.1186/1471-2105-12-231Author
Kim, Su Yeon ; Lohmueller, Kirk E ; Albrechtsen, Anders ; Li, Yingrui ; Korneliussen, Thorfinn Sand ; Tian, Geng ; Grarup, Niels ; Jiang, Tao ; Andersen, Gitte ; Witte, Daniel ; Jorgensen, Torben ; Hansen, Torben ; Pedersen, Oluf ; Wang, Jun ; Nielsen, Rasmus. / Estimation of allele frequency and association mapping using next-generation sequencing data. I: B M C Bioinformatics. 2011 ; Bind 12. s. 231.
Bibtex
@article{fde68434340848d792fe0bd8537f9037,
title = "Estimation of allele frequency and association mapping using next-generation sequencing data",
abstract = "Estimation of allele frequency is of fundamental importance in population genetic analyses and in association mapping. In most studies using next-generation sequencing, a cost effective approach is to use medium or low-coverage data (e.g., <15X). However, SNP calling and allele frequency estimation in such studies is associated with substantial statistical uncertainty because of varying coverage and high error rates.",
keywords = "Gene Frequency, Genetics, Population, Genotype, High-Throughput Nucleotide Sequencing, Humans, Likelihood Functions, Polymorphism, Single Nucleotide, Sequence Analysis, DNA",
author = "Kim, {Su Yeon} and Lohmueller, {Kirk E} and Anders Albrechtsen and Yingrui Li and Korneliussen, {Thorfinn Sand} and Geng Tian and Niels Grarup and Tao Jiang and Gitte Andersen and Daniel Witte and Torben Jorgensen and Torben Hansen and Oluf Pedersen and Jun Wang and Rasmus Nielsen",
year = "2011",
doi = "10.1186/1471-2105-12-231",
language = "English",
volume = "12",
pages = "231",
journal = "B M C Bioinformatics",
issn = "1471-2105",
publisher = "BioMed Central Ltd.",
}
RIS
TY - JOUR
T1 - Estimation of allele frequency and association mapping using next-generation sequencing data
AU - Kim, Su Yeon
AU - Lohmueller, Kirk E
AU - Albrechtsen, Anders
AU - Li, Yingrui
AU - Korneliussen, Thorfinn Sand
AU - Tian, Geng
AU - Grarup, Niels
AU - Jiang, Tao
AU - Andersen, Gitte
AU - Witte, Daniel
AU - Jorgensen, Torben
AU - Hansen, Torben
AU - Pedersen, Oluf
AU - Wang, Jun
AU - Nielsen, Rasmus
PY - 2011
Y1 - 2011
N2 - Estimation of allele frequency is of fundamental importance in population genetic analyses and in association mapping. In most studies using next-generation sequencing, a cost effective approach is to use medium or low-coverage data (e.g., <15X). However, SNP calling and allele frequency estimation in such studies is associated with substantial statistical uncertainty because of varying coverage and high error rates.
AB - Estimation of allele frequency is of fundamental importance in population genetic analyses and in association mapping. In most studies using next-generation sequencing, a cost effective approach is to use medium or low-coverage data (e.g., <15X). However, SNP calling and allele frequency estimation in such studies is associated with substantial statistical uncertainty because of varying coverage and high error rates.
KW - Gene Frequency
KW - Genetics, Population
KW - Genotype
KW - High-Throughput Nucleotide Sequencing
KW - Humans
KW - Likelihood Functions
KW - Polymorphism, Single Nucleotide
KW - Sequence Analysis, DNA
U2 - 10.1186/1471-2105-12-231
DO - 10.1186/1471-2105-12-231
M3 - Journal article
C2 - 21663684
VL - 12
SP - 231
JO - B M C Bioinformatics
JF - B M C Bioinformatics
SN - 1471-2105
ER -
