These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 31730669)

  • 81. Ion Torrent sequencing as a tool for mutation discovery in the flax (Linum usitatissimum L.) genome.
    Galindo-González L; Pinzón-Latorre D; Bergen EA; Jensen DC; Deyholos MK
    Plant Methods; 2015; 11():19. PubMed ID: 25788971
    [TBL] [Abstract][Full Text] [Related]  

  • 82. Human whole mitochondrial genome sequencing and analysis: optimization of the experimental workflow.
    Sukser V; Korolija M; Račić I; Rožić S; Barbarić L
    Croat Med J; 2022 Jun; 63(3):224-230. PubMed ID: 35722691
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Comparative analysis of novel MGISEQ-2000 sequencing platform vs Illumina HiSeq 2500 for whole-genome sequencing.
    Korostin D; Kulemin N; Naumov V; Belova V; Kwon D; Gorbachev A
    PLoS One; 2020; 15(3):e0230301. PubMed ID: 32176719
    [TBL] [Abstract][Full Text] [Related]  

  • 84. Inexpensive and Highly Reproducible Cloud-Based Variant Calling of 2,535 Human Genomes.
    Shringarpure SS; Carroll A; De La Vega FM; Bustamante CD
    PLoS One; 2015; 10(6):e0129277. PubMed ID: 26110529
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Evaluating methods for Avian avulavirus-1 whole genome sequencing.
    Tal S; Ben Izhak M; Wachtel C; Wiseman A; Braun T; Yechezkel E; Golan E; Hadas R; Turjeman A; Banet-Noach C; Bronstein M; Lublin A; Berman E; Raviv Z; Pirak M; Klement E; Louzoun Y
    Gene X; 2019 Feb; 1():100004. PubMed ID: 32550541
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Successful preimplantation genetic diagnosis by targeted next-generation sequencing on an ion torrent personal genome machine platform.
    Hao Y; Chen D; Zhang Z; Zhou P; Cao Y; Wei Z; Xu X; Chen B; Zou W; Lv M; Ji D; He X
    Oncol Lett; 2018 Apr; 15(4):4296-4302. PubMed ID: 29541197
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Measurement error and variant-calling in deep Illumina sequencing of HIV.
    Howison M; Coetzer M; Kantor R
    Bioinformatics; 2019 Jun; 35(12):2029-2035. PubMed ID: 30407489
    [TBL] [Abstract][Full Text] [Related]  

  • 88. Cost-effective straightforward method for captured whole mitogenome sequencing of ancient DNA.
    Senovska A; Drozdova E; Vaculik O; Pardy F; Brzobohata K; Fialova D; Smerda J; Kos P
    Forensic Sci Int; 2021 Feb; 319():110638. PubMed ID: 33340848
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Automated library preparation for whole genome sequencing by centrifugal microfluidics.
    Hess JF; Hess ME; Zengerle R; Paust N; Boerries M; Hutzenlaub T
    Anal Chim Acta; 2021 Oct; 1182():338954. PubMed ID: 34602197
    [TBL] [Abstract][Full Text] [Related]  

  • 90. The lot-to-lot variability in the mitochondrial genome of controls.
    Cihlar JC; Peters D; Strobl C; Parson W; Budowle B
    Forensic Sci Int Genet; 2020 Jul; 47():102298. PubMed ID: 32464353
    [TBL] [Abstract][Full Text] [Related]  

  • 91. PipeIT2: Somatic Variant Calling Workflow for Ion Torrent Sequencing Data.
    Garofoli A; Schnidrig D; Ng CKY
    Methods Mol Biol; 2022; 2493():195-204. PubMed ID: 35751816
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Evaluating methods for Avian avulavirus-1 whole genome sequencing.
    Tal S; Ben Izhak M; Wachtel C; Wiseman A; Braun T; Yechezkel E; Golan E; Hadas R; Turjeman A; Banet-Noach C; Bronstein M; Lublin A; Berman E; Raviv Z; Pirak M; Klement E; Louzoun Y
    Gene; 2019; 721S():100004. PubMed ID: 34530998
    [TBL] [Abstract][Full Text] [Related]  

  • 93. The Easy-to-Use SARS-CoV-2 Assembler for Genome Sequencing: Development Study.
    Rueca M; Giombini E; Messina F; Bartolini B; Di Caro A; Capobianchi MR; Gruber CE
    JMIR Bioinform Biotechnol; 2022; 3(1):e31536. PubMed ID: 35309411
    [TBL] [Abstract][Full Text] [Related]  

  • 94. German-Wide Interlaboratory Study Compares Consistency, Accuracy and Reproducibility of Whole-Genome Short Read Sequencing.
    Uelze L; Borowiak M; Bönn M; Brinks E; Deneke C; Hankeln T; Kleta S; Murr L; Stingl K; Szabo K; Tausch SH; Wöhlke A; Malorny B
    Front Microbiol; 2020; 11():573972. PubMed ID: 33013811
    [TBL] [Abstract][Full Text] [Related]  

  • 95. Adapting SureSelect enrichment protocol to the Ion Torrent S5 platform in molecular diagnostics of craniosynostosis.
    Bukowska-Olech E; Popiel D; Koczyk G; Sowińska-Seidler A; Socha M; Wojciechowicz B; Dawidziuk A; Larysz D; Jamsheer A
    Sci Rep; 2020 Mar; 10(1):4159. PubMed ID: 32139749
    [TBL] [Abstract][Full Text] [Related]  

  • 96. Genome skimming is a low-cost and robust strategy to assemble complete mitochondrial genomes from ethanol preserved specimens in biodiversity studies.
    Trevisan B; Alcantara DMC; Machado DJ; Marques FPL; Lahr DJG
    PeerJ; 2019; 7():e7543. PubMed ID: 31565556
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Replicate whole-genome next-generation sequencing data derived from Caucasian donor saliva samples.
    Hansen MH; Nyvold CG
    Data Brief; 2021 Oct; 38():107349. PubMed ID: 34522736
    [TBL] [Abstract][Full Text] [Related]  

  • 98. A Protocol for mtGenome Analysis on Large Sample Numbers.
    Hamoy IG; Ribeiro-Dos-Santos AM; Alvarez L; Barbosa S; Silva A; Santos S; Gusmão L; Ribeiro-Dos-Santos A
    Bioinform Biol Insights; 2014; 8():127-34. PubMed ID: 25002812
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Using VAAST to Identify Disease-Associated Variants in Next-Generation Sequencing Data.
    Kennedy B; Kronenberg Z; Hu H; Moore B; Flygare S; Reese MG; Jorde LB; Yandell M; Huff C
    Curr Protoc Hum Genet; 2014 Apr; 81():6.14.1-6.14.25. PubMed ID: 24763993
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Strategies for achieving high sequencing accuracy for low diversity samples and avoiding sample bleeding using illumina platform.
    Mitra A; Skrzypczak M; Ginalski K; Rowicka M
    PLoS One; 2015; 10(4):e0120520. PubMed ID: 25860802
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.