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Refinado por: assunto: Genetics remover
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HIVID: An efficient method to detect HBV integration using low coverage sequencing
HIVID: An efficient method to detect HBV integration using low coverage sequencing
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HIVID: An efficient method to detect HBV integration using low coverage sequencing

Li, Weiyang ; Zeng, Xi ; Lee, Nikki P. ; Liu, Xiao ; Chen, Shengpei ; Guo, Bing ; Yi, Shang ; Zhuang, Xuehan ; Chen, Fang ; Wang, Guan ; Poon, Ronnie T. ; Fan, Sheung Tat ; Mao, Mao ; Li, Yingrui ; Li, Songgang ; Wang, Jun ; JianWang ; Xu, Xun ; Jiang, Hui ; Zhang, Xiuqing

Genomics (San Diego, Calif.), 2013-10, Vol.102 (4), p.338-344 [Periódico revisado por pares]

United States: Elsevier Inc

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12
Classification of factors involved in nonreportable results of noninvasive prenatal testing (NIPT) and prediction of success rate of second NIPT
Classification of factors involved in nonreportable results of noninvasive prenatal testing (NIPT) and prediction of success rate of second NIPT
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Classification of factors involved in nonreportable results of noninvasive prenatal testing (NIPT) and prediction of success rate of second NIPT

Suzumori, Nobuhiro ; Sekizawa, Akihiko ; Takeda, Eri ; Samura, Osamu ; Sasaki, Aiko ; Akaishi, Rina ; Wada, Seiji ; Hamanoue, Haruka ; Hirahara, Fumiki ; Kuriki, Hiroko ; Sawai, Hideaki ; Nakamura, Hiroaki ; Yamada, Takahiro ; Miura, Kiyonori ; Masuzaki, Hideaki ; Yamashita, Takahiro ; Kamei, Yoshimasa ; Namba, Akira ; Murotsuki, Jun ; Tanemoto, Tomohiro ; Fukushima, Akimune ; Haino, Kazufumi ; Tairaku, Shinya ; Matsubara, Keiichi ; Maeda, Kazutoshi ; Kaji, Takashi ; Ogawa, Masanobu ; Osada, Hisao ; Nishizawa, Haruki ; Okamoto, Yoko ; Kanagawa, Takeshi ; Kakigano, Aiko ; Endo, Masayuki ; Kitagawa, Michihiro ; Ogawa, Masaki ; Izumi, Shunichiro ; Katagiri, Yukiko ; Takeshita, Naoki ; Kasai, Yasuyo ; Naruse, Katsuhiko ; Neki, Reiko ; Masuyama, Hisashi ; Hyodo, Maki ; Kawano, Yukie ; Ohba, Takashi ; Ichizuka, Kiyotake ; Nagamatsu, Takeshi ; Watanabe, Atsushi ; Nishikawa, Naomi ; Hamajima, Naoki ; Shirato, Nahoko ; Yotsumoto, Junko ; Nishiyama, Miyuki ; Koide, Keiko ; Hirose, Tatsuko ; Sago, Haruhiko

Prenatal diagnosis, 2019-01, Vol.39 (2), p.100-106 [Periódico revisado por pares]

England

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13
Sequencing-based methods and resources to study antimicrobial resistance
Sequencing-based methods and resources to study antimicrobial resistance
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Sequencing-based methods and resources to study antimicrobial resistance

Boolchandani, Manish ; D'Souza, Alaric W ; Dantas, Gautam

Nature reviews. Genetics, 2019-06, Vol.20 (6), p.356-370 [Periódico revisado por pares]

England: Nature Publishing Group

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14
Comparison and evaluation of two exome capture kits and sequencing platforms for variant calling
Comparison and evaluation of two exome capture kits and sequencing platforms for variant calling
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Comparison and evaluation of two exome capture kits and sequencing platforms for variant calling

Zhang, Guoqiang ; Wang, Jianfeng ; Yang, Jin ; Li, Wenjie ; Deng, Yutian ; Li, Jing ; Huang, Jun ; Hu, Songnian ; Zhang, Bing

BMC genomics, 2015-08, Vol.16 (1), p.581-581, Article 581 [Periódico revisado por pares]

England: BioMed Central Ltd

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15
Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion
Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion
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Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion

Abou Tayoun, Ahmad N. ; Pesaran, Tina ; DiStefano, Marina T. ; Oza, Andrea ; Rehm, Heidi L. ; Biesecker, Leslie G. ; Harrison, Steven M.

Human mutation, 2018-11, Vol.39 (11), p.1517-1524 [Periódico revisado por pares]

United States: Wiley Periodicals Inc

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16
Advancements in Next-Generation Sequencing
Advancements in Next-Generation Sequencing
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Advancements in Next-Generation Sequencing

Levy, Shawn E ; Myers, Richard M

Annual review of genomics and human genetics, 2016-08, Vol.17 (1), p.95-115 [Periódico revisado por pares]

United States: Annual Reviews

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17
Sequencing-based diagnostics for pediatric genetic diseases: progress and potential
Sequencing-based diagnostics for pediatric genetic diseases: progress and potential
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Sequencing-based diagnostics for pediatric genetic diseases: progress and potential

Abou Tayoun, Ahmad N. ; Krock, Bryan ; Spinner, Nancy B.

Expert review of molecular diagnostics, 2016-09, Vol.16 (9), p.987-999 [Periódico revisado por pares]

England: Taylor & Francis

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18
Efficient and unique cobarcoding of second-generation sequencing reads from long DNA molecules enabling cost-effective and accurate sequencing, haplotyping, and de novo assembly
Efficient and unique cobarcoding of second-generation sequencing reads from long DNA molecules enabling cost-effective and accurate sequencing, haplotyping, and de novo assembly
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Efficient and unique cobarcoding of second-generation sequencing reads from long DNA molecules enabling cost-effective and accurate sequencing, haplotyping, and de novo assembly

Wang, Ou ; Chin, Robert ; Cheng, Xiaofang ; Wu, Michelle Ka Yan ; Mao, Qing ; Tang, Jingbo ; Sun, Yuhui ; Anderson, Ellis ; Lam, Han K ; Chen, Dan ; Zhou, Yujun ; Wang, Linying ; Fan, Fei ; Zou, Yan ; Xie, Yinlong ; Zhang, Rebecca Yu ; Drmanac, Snezana ; Nguyen, Darlene ; Xu, Chongjun ; Villarosa, Christian ; Gablenz, Scott ; Barua, Nina ; Nguyen, Staci ; Tian, Wenlan ; Liu, Jia Sophie ; Wang, Jingwan ; Liu, Xiao ; Qi, Xiaojuan ; Chen, Ao ; Wang, He ; Dong, Yuliang ; Zhang, Wenwei ; Alexeev, Andrei ; Yang, Huanming ; Wang, Jian ; Kristiansen, Karsten ; Xu, Xun ; Drmanac, Radoje ; Peters, Brock A

Genome research, 2019-05, Vol.29 (5), p.798-808 [Periódico revisado por pares]

United States: Cold Spring Harbor Laboratory Press

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19
Computational and analytical challenges in single-cell transcriptomics
Computational and analytical challenges in single-cell transcriptomics
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Computational and analytical challenges in single-cell transcriptomics

Stegle, Oliver ; Teichmann, Sarah A ; Marioni, John C

Nature reviews. Genetics, 2015-03, Vol.16 (3), p.133-145 [Periódico revisado por pares]

England: Nature Publishing Group

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20
Sequencing pools of individuals - mining genome-wide polymorphism data without big funding
Sequencing pools of individuals - mining genome-wide polymorphism data without big funding
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Sequencing pools of individuals - mining genome-wide polymorphism data without big funding

Schlötterer, Christian ; Tobler, Raymond ; Kofler, Robert ; Nolte, Viola

Nature reviews. Genetics, 2014-11, Vol.15 (11), p.749-763 [Periódico revisado por pares]

England: Nature Publishing Group

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Deste Autor:

  1. Bertola, D
  2. Souza, B
  3. Yamamoto, G
  4. Jorge, A
  5. Pessente, G

Neste Assunto:

  1. Genetics
  2. Genetics
  3. Science & Technology
  4. High-Throughput Nucleotide Sequencing
  5. Life Sciences & Biomedicine

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