SgD-CNV, a database for common and rare copy number variants in three Asian populations

SgD-CNV, a database for common and rare copy number variants in three Asian populations

10.1002/humu.21601

Saved in:

書目詳細資料
Main Authors:	Xu, H., Poh, W.-T., Sim, X., Ong, R.T.-H., Suo, C., Tay, W.-T., Khor, C.-C., Seielstad, M., Liu, J., Aung, T., Tai, E.-S., Wong, T.-Y., Chia, K.-S., Teo, Y.-Y.
其他作者:	STATISTICS & APPLIED PROBABILITY
格式:	Article
出版:	2014
主題:	Copy number variant Population genetics Rare variant
在線閱讀:	http://scholarbank.nus.edu.sg/handle/10635/53162
標簽:	添加標簽沒有標簽, 成為第一個標記此記錄!

相似書籍

Approaches to multiple rare variants analysis in sequencing association studies
由: SERGII ZAKHAROV
出版: (2014)

The pursuit of genome-wide association studies: Where are we now
由: Ku, C.S., et al.
出版: (2011)

The pursuit of genome-wide association studies: Where are we now
由: Ku, C.S., et al.
出版: (2011)

Statistical Methods for the Detection and Analyses of Structural Variants in the Human Genome
由: TEO SHU MEI
出版: (2012)

A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals
由: Teo, S.-M., et al.
出版: (2014)

Comparison of similarity-based tests and pooling strategies for rare variants
由: Zakharov, S., et al.
出版: (2014)

Exon sequencing and association analysis of EPHX1 genetic variants with maintenance warfarin dose in a multiethnic Asian population
由: Chan, S.L., et al.
出版: (2014)

A fast collapsed data method for estimating haplotype frequencies from pooled genotype data with applications to the study of rare variants
由: Kuk, A.Y.C., et al.
出版: (2014)

An EM algorithm based on an internal list for estimating haplotype distributions of rare variants from pooled genotype data
由: Kuk, A.Y.C., et al.
出版: (2014)

A stepwise likelihood ratio test procedure for rare variant selection in case-control studies
由: Kuk, A.Y.C., et al.
出版: (2014)

Variant angina in a 6-year-old boy
由: Lim, C.W.T., et al.
出版: (2011)

Varied pathological and therapeutic response effects associated with CHCHD2 mutant and risk variants
由: Tio M., et al.
出版: (2018)

LRRK2 variant associated with Alzheimer's disease
由: Zhao, Y., et al.
出版: (2014)

Pathogenicity of LRRK2 P755L variant in Parkinson's disease
由: Tan E.-K., et al.
出版: (2018)

Essential tremor and the common LRRK2 G2385R variant
由: Tan E.-K., et al.
出版: (2018)

A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy
由: Horvat C., et al.
出版: (2018)

Rapid displacement of SARS-CoV-2 variant Delta by Omicron revealed by allele-specific PCR in wastewater
由: Lee, Wei Lin, et al.
出版: (2023)

Identification of a loss-of-function inducible degrader of the low-density lipoprotein receptor variant in individuals with low circulating low-density lipoprotein
由: Sorrentino, Vincenzo, et al.
出版: (2024)

Gene copy number variation in natural populations of Plasmodium falciparum in Eastern Africa
由: Simam, Joan, et al.
出版: (2018)

Identification of hemoglobin variants in samples received for glycated hemoglobin testing
由: Saw, S., et al.
出版: (2016)

Histone variants in skeletal myogenesis.
由: NANDINI KARTHIK, et al.
出版: (2020)

Case-control analysis of leucine-rich repeat kinase 2 protective variants in Alzheimer's disease
由: Ng A.S.L., et al.
出版: (2018)

Case control analysis of LRRK2 Gly2385Arg in Alzheimer's disease
由: Tan, E.K., et al.
出版: (2016)

Statistical methods for analysis and integration of microarray data
由: SUO CHEN
出版: (2011)

A flow-based approach for variant parametric types
由: Chin, W.-N., et al.
出版: (2013)

A flow-based approach for variant parametric types
由: Chin, W.-N., et al.
出版: (2013)

Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants
由: Wong, Colin C. X. F., et al.
出版: (2019)

Copy number variation in Thai population
由: Bhoom Suktitipat, et al.
出版: (2015)

NanoVar : accurate characterization of patients' genomic structural variants using low-depth nanopore sequencing
由: Tham, Cheng Yong, et al.
出版: (2021)

Handling variant requirements in domain modeling
由: Jarzabek, S., et al.
出版: (2013)

Genomic copy number variations in three southeast Asian populations
由: Ku, C.-S., et al.
出版: (2011)

Genetic variants in sporadic parkinson's disease: East vs west
由: Peeraully T., et al.
出版: (2018)

Histone variant H3.3 promotes metastasis in alveolar rhabdomyosarcoma.
由: Karthik, Nandini, et al.
出版: (2023)

Systematic evaluation of genes and genetic variants associated with type 1 diabetes susceptibility
由: Boehm, Bernhard Otto, et al.
出版: (2018)

LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China
由: Zhang, Z., et al.
出版: (2015)

Single gene contributions: Genetic variants of peroxisome proliferator-activated receptor (isoforms α, β/δ and γ) and mechanisms of dyslipidemias
由: Yong, E.L., et al.
出版: (2011)

Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's disease
由: Foo J.N., et al.
出版: (2018)

Association of molecular variants of luteinizing hormone with male infertility
由: Ramanujam, L.N., et al.
出版: (2013)

Methods for DNA Copy Number Variation Analysis Using High-Throughput Sequencing
由: XIE CHAO
出版: (2011)

Avoiding some common preprocessing pitfalls with feature queries
由: Jarzabek, S., et al.
出版: (2013)