Wu JY - Search Results

1

Copy number variant hotspots in Han Taiwanese population induced pluripotent stem cell lines - lessons from establishing the Taiwan human disease iPSC Consortium Bank.

Huang CY, Li LH, Hsu WT, Cheng YC, Nicholson MW, Liu CL, Ting CY, Ko HW, Syu SH, Wen CH, Yan Z, Huang HP, Su HL, Chiang PM, Shen CN, Chen HF, Yen BLJ, Lu HE, Hwang SM, Chiou SH, Ho HN, Wu JY, Kamp TJ, Wu JC, Hsieh PCH. Huang CY, et al. Among authors: wu jy, wu jc. J Biomed Sci. 2020 Sep 4;27(1):92. doi: 10.1186/s12929-020-00682-7. J Biomed Sci. 2020. PMID: 32887585 Free PMC article.

2

Long contiguous stretches of homozygosity in the human genome.

Li LH, Ho SF, Chen CH, Wei CY, Wong WC, Li LY, Hung SI, Chung WH, Pan WH, Lee MT, Tsai FJ, Chang CF, Wu JY, Chen YT. Li LH, et al. Among authors: wu jy. Hum Mutat. 2006 Nov;27(11):1115-21. doi: 10.1002/humu.20399. Hum Mutat. 2006. PMID: 16955415

3

MPDA: microarray pooled DNA analyzer.

Yang HC, Huang MC, Li LH, Lin CH, Yu AL, Diccianni MB, Wu JY, Chen YT, Fann CS. Yang HC, et al. Among authors: wu jy. BMC Bioinformatics. 2008 Apr 15;9:196. doi: 10.1186/1471-2105-9-196. BMC Bioinformatics. 2008. PMID: 18412951 Free PMC article.

4

Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.

Lin CH, Huang MC, Li LH, Wu JY, Chen YT, Fann CS. Lin CH, et al. Among authors: wu jy. Hum Mutat. 2008 Aug;29(8):1055-62. doi: 10.1002/humu.20760. Hum Mutat. 2008. PMID: 18470944

5

A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan.

Lin CH, Li LH, Ho SF, Chuang TP, Wu JY, Chen YT, Fann CS. Lin CH, et al. Among authors: wu jy. BMC Genet. 2008 Dec 24;9:92. doi: 10.1186/1471-2156-9-92. BMC Genet. 2008. PMID: 19108714 Free PMC article.

6

A new familial insertion, ins(18;9)(q12.2;q33.1q31.1) with a 9q31.1-9q33.1 deletion in a girl with a cleft lip and palate.

Chien SC, Li YC, Li LH, Wu JY, Hsu PC, Shi SL, Tsai FJ, Lin CC. Chien SC, et al. Among authors: wu jy. Am J Med Genet A. 2010 Jul;152A(7):1862-7. doi: 10.1002/ajmg.a.33452. Am J Med Genet A. 2010. PMID: 20583161 No abstract available.

7

A new analysis tool for individual-level allele frequency for genomic studies.

Yang HC, Lin HC, Huang MC, Li LH, Pan WH, Wu JY, Chen YT. Yang HC, et al. Among authors: wu jy. BMC Genomics. 2010 Jul 5;11:415. doi: 10.1186/1471-2164-11-415. BMC Genomics. 2010. PMID: 20602748 Free PMC article.

8

Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome.

Chang CF, Li LH, Wang CH, Tsai FJ, Chen TC, Wu JY, Chen YT, Tsai AC. Chang CF, et al. Among authors: wu jy. Am J Med Genet A. 2010 Sep;152A(9):2365-71. doi: 10.1002/ajmg.a.33580. Am J Med Genet A. 2010. PMID: 20803649

9

SAQC: SNP array quality control.

Yang HC, Lin HC, Kang M, Chen CH, Lin CW, Li LH, Wu JY, Chen YT, Pan WH. Yang HC, et al. Among authors: wu jy. BMC Bioinformatics. 2011 Apr 18;12:100. doi: 10.1186/1471-2105-12-100. BMC Bioinformatics. 2011. PMID: 21501472 Free PMC article.

10

An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.

Huang MC, Chuang TP, Chen CH, Wu JY, Chen YT, Li LH, Yang HC. Huang MC, et al. Among authors: wu jy. BMC Genomics. 2016 Mar 31;17:266. doi: 10.1186/s12864-016-2478-8. BMC Genomics. 2016. PMID: 27029637 Free PMC article.

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