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11
Genomics‐based non‐invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women
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Genomics‐based non‐invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women

Badeau, Mylène ; Lindsay, Carmen ; Blais, Jonatan ; Nshimyumukiza, Leon ; Takwoingi, Yemisi ; Langlois, Sylvie ; Légaré, France ; Giguère, Yves ; Turgeon, Alexis F ; Witteman, William ; Rousseau, François ; Rousseau, François

Cochrane database of systematic reviews, 2017-11, Vol.2017 (11), p.CD011767 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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12
Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication
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Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication

Tian, Weifang ; Yuan, Yangyang ; Yuan, Erfeng ; Zhang, Linlin ; Liu, Ling ; Li, Ying ; Guo, Jing ; Cui, Xueyin ; Li, Pengyun ; Cui, Shihong

European journal of medical research, 2023-08, Vol.28 (1), p.1-304, Article 304 [Periódico revisado por pares]

London: BioMed Central Ltd

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13
Next generation sequencing for miRNA profile of spleen CD4 + T cells in the murine model of acute asthma
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Next generation sequencing for miRNA profile of spleen CD4 + T cells in the murine model of acute asthma

Liu, Ye ; Chen, Zhongqi ; Xu, Kun ; Wang, Zhengxia ; Wu, Chaojie ; Sun, Zhixiao ; Ji, Ningfei ; Huang, Mao ; Zhang, Mingshun

Epigenomics, 2018-08, Vol.10 (8), p.1071-1083 [Periódico revisado por pares]

England: Future Medicine Ltd

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14
A Novel System for the Detection of Spontaneous Abortion-Causing Aneuploidy and Its Erroneous Chromosome Origins through the Combination of Low-Pass Copy Number Variation Sequencing and NGS-Based STR Tests
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Artigo
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A Novel System for the Detection of Spontaneous Abortion-Causing Aneuploidy and Its Erroneous Chromosome Origins through the Combination of Low-Pass Copy Number Variation Sequencing and NGS-Based STR Tests

Lei, Caixia ; Liao, Kai ; Zhao, Yuwei ; Long, Zhoukai ; Zhu, Saijuan ; Wu, Junping ; Xiao, Min ; Zhou, Jing ; Zhang, Shuo ; Li, Lianbin ; Zhu, Yijian ; Lu, Daru ; Yang, Jingmin ; Sun, Xiaoxi

Journal of clinical medicine, 2023-02, Vol.12 (5), p.1809 [Periódico revisado por pares]

Switzerland: MDPI AG

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15
Insight into the genomic diversity: Genome wide association study unveils the SNP diversity in horsgram germplsam
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Insight into the genomic diversity: Genome wide association study unveils the SNP diversity in horsgram germplsam

Sharma, Ankita ; Chahota, Rakesh Kumar

South African journal of botany, 2024-05, Vol.168, p.406-416 [Periódico revisado por pares]

Elsevier B.V

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16
Persistence of Human Immunodeficiency Virus-1 Drug Resistance Mutations in Proviral Deoxyribonucleic Acid After Virologic Failure of Efavirenz-Containing Antiretroviral Regimens
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Artigo
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Persistence of Human Immunodeficiency Virus-1 Drug Resistance Mutations in Proviral Deoxyribonucleic Acid After Virologic Failure of Efavirenz-Containing Antiretroviral Regimens

De La Cruz, Justin ; Vardhanbhuti, Saran ; Sahoo, Malaya K ; Rovner, Robert ; Bosch, Ronald J ; Manasa, Justen ; Katzenstein, David A ; Pinsky, Benjamin A

Open forum infectious diseases, 2019-03, Vol.6 (3), p.ofz034-ofz034 [Periódico revisado por pares]

US: Oxford University Press

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17
TCC: an R package for comparing tag count data with robust normalization strategies
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TCC: an R package for comparing tag count data with robust normalization strategies

Sun, Jianqiang ; Nishiyama, Tomoaki ; Shimizu, Kentaro ; Kadota, Koji

BMC bioinformatics, 2013-07, Vol.14 (1), p.219-219, Article 219 [Periódico revisado por pares]

England: BioMed Central Ltd

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18
Characterization of exosomal RNAs derived from human gastric cancer cells by deep sequencing
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Characterization of exosomal RNAs derived from human gastric cancer cells by deep sequencing

Ren, Jia ; Zhou, Quan ; Li, Hao ; Li, Jianfang ; Pang, Li ; Su, Liping ; Gu, Qinlong ; Zhu, Zhenggang ; Liu, Bingya

Tumor biology, 2017-04, Vol.39 (4), p.1010428317695012-1010428317695012 [Periódico revisado por pares]

London, England: SAGE Publications

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19
A Review of Health Economic Studies Comparing Traditional and Massively Parallel Sequencing Diagnostic Pathways for Suspected Genetic Disorders
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A Review of Health Economic Studies Comparing Traditional and Massively Parallel Sequencing Diagnostic Pathways for Suspected Genetic Disorders

Fahr, Patrick ; Buchanan, James ; Wordsworth, Sarah

PharmacoEconomics, 2020-02, Vol.38 (2), p.143-158 [Periódico revisado por pares]

Cham: Springer International Publishing

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20
Compositional Bias in Naïve and Chemically-modified Phage-Displayed Libraries uncovered by Paired-end Deep Sequencing
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Compositional Bias in Naïve and Chemically-modified Phage-Displayed Libraries uncovered by Paired-end Deep Sequencing

He, Bifang ; Tjhung, Katrina F ; Bennett, Nicholas J ; Chou, Ying ; Rau, Andrea ; Huang, Jian ; Derda, Ratmir

Scientific reports, 2018-01, Vol.8 (1), p.1214-14, Article 1214 [Periódico revisado por pares]

England: Nature Publishing Group

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