219 related articles for article (PubMed ID: 30141054)
1. Next-Generation Sequencing and Mutational Analysis: Implications for Genes Encoding LINC Complex Proteins.
Nagy PL; Worman HJ
Methods Mol Biol; 2018; 1840():321-336. PubMed ID: 30141054
[TBL] [Abstract][Full Text] [Related]
2. More Pitfalls Related to Next-generation Sequencing (NGS).
Sorscher S
Am J Clin Oncol; 2016 Aug; 39(4):424. PubMed ID: 27465427
[No Abstract] [Full Text] [Related]
3. Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients.
Lim EC; Brett M; Lai AH; Lee SP; Tan ES; Jamuar SS; Ng IS; Tan EC
Hum Genomics; 2015 Dec; 9():33. PubMed ID: 26666243
[TBL] [Abstract][Full Text] [Related]
4. Tilling by sequencing.
Tsai H; Ngo K; Lieberman M; Missirian V; Comai L
Methods Mol Biol; 2015; 1284():359-80. PubMed ID: 25757782
[TBL] [Abstract][Full Text] [Related]
5. Amplicon-Based Targeted Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Tissue.
Strengman E; Barendrecht-Smouter FAS; de Voijs C; de Vree P; Nijman IJ; de Leng WWJ
Methods Mol Biol; 2019; 1908():1-17. PubMed ID: 30649717
[TBL] [Abstract][Full Text] [Related]
6. mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing.
Li J; Jiang Y; Wang T; Chen H; Xie Q; Shao Q; Ran X; Xia K; Sun ZS; Wu J
J Med Genet; 2015 Apr; 52(4):275-81. PubMed ID: 25596308
[TBL] [Abstract][Full Text] [Related]
7. Lake Louise mutation detection meeting 2013: clinical translation of next-generation sequencing requires optimization of workflows and interpretation of variants.
Smith A; Boycott KM; Jarinova O
Hum Mutat; 2014 Feb; 35(2):265-9. PubMed ID: 24282140
[TBL] [Abstract][Full Text] [Related]
8. Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
LaDuca H; Farwell KD; Vuong H; Lu HM; Mu W; Shahmirzadi L; Tang S; Chen J; Bhide S; Chao EC
PLoS One; 2017; 12(2):e0170843. PubMed ID: 28152038
[TBL] [Abstract][Full Text] [Related]
9. Library Construction for Mutation Identification by Whole-Genome Sequencing.
Smith HE
Methods Mol Biol; 2015; 1327():1-9. PubMed ID: 26423963
[TBL] [Abstract][Full Text] [Related]
10. Challenges in exome analysis by LifeScope and its alternative computational pipelines.
Pranckevičiene E; Rančelis T; Pranculis A; Kučinskas V
BMC Res Notes; 2015 Sep; 8():421. PubMed ID: 26346699
[TBL] [Abstract][Full Text] [Related]
11. Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease.
Dilliott AA; Farhan SMK; Ghani M; Sato C; Liang E; Zhang M; McIntyre AD; Cao H; Racacho L; Robinson JF; Strong MJ; Masellis M; Bulman DE; Rogaeva E; Lang A; Tartaglia C; Finger E; Zinman L; Turnbull J; Freedman M; Swartz R; Black SE; Hegele RA
J Vis Exp; 2018 Apr; (134):. PubMed ID: 29683450
[TBL] [Abstract][Full Text] [Related]
12. Next-generation sequencing in the clinic: promises and challenges.
Xuan J; Yu Y; Qing T; Guo L; Shi L
Cancer Lett; 2013 Nov; 340(2):284-95. PubMed ID: 23174106
[TBL] [Abstract][Full Text] [Related]
13. Development and analytical validation of a 25-gene next generation sequencing panel that includes the BRCA1 and BRCA2 genes to assess hereditary cancer risk.
Judkins T; Leclair B; Bowles K; Gutin N; Trost J; McCulloch J; Bhatnagar S; Murray A; Craft J; Wardell B; Bastian M; Mitchell J; Chen J; Tran T; Williams D; Potter J; Jammulapati S; Perry M; Morris B; Roa B; Timms K
BMC Cancer; 2015 Apr; 15():215. PubMed ID: 25886519
[TBL] [Abstract][Full Text] [Related]
14. Opportunities and challenges of whole-genome and -exome sequencing.
Petersen BS; Fredrich B; Hoeppner MP; Ellinghaus D; Franke A
BMC Genet; 2017 Feb; 18(1):14. PubMed ID: 28193154
[TBL] [Abstract][Full Text] [Related]
15. MutAid: Sanger and NGS Based Integrated Pipeline for Mutation Identification, Validation and Annotation in Human Molecular Genetics.
Pandey RV; Pabinger S; Kriegner A; Weinhäusel A
PLoS One; 2016; 11(2):e0147697. PubMed ID: 26840129
[TBL] [Abstract][Full Text] [Related]
16. From Wet-Lab to Variations: Concordance and Speed of Bioinformatics Pipelines for Whole Genome and Whole Exome Sequencing.
Laurie S; Fernandez-Callejo M; Marco-Sola S; Trotta JR; Camps J; Chacón A; Espinosa A; Gut M; Gut I; Heath S; Beltran S
Hum Mutat; 2016 Dec; 37(12):1263-1271. PubMed ID: 27604516
[TBL] [Abstract][Full Text] [Related]
17. Identification of mutations in zebrafish using next-generation sequencing.
Henke K; Bowen ME; Harris MP
Curr Protoc Mol Biol; 2013 Oct; 104():7.13.1-7.13.33. PubMed ID: 24510885
[TBL] [Abstract][Full Text] [Related]
18. Integrated next-generation sequencing analysis of whole exome and 409 cancer-related genes.
Shimoda Y; Nagashima T; Urakami K; Tanabe T; Saito J; Naruoka A; Serizawa M; Mochizuki T; Ohshima K; Ohnami S; Ohnami S; Kusuhara M; Yamaguchi K
Biomed Res; 2016; 37(6):367-379. PubMed ID: 28003584
[TBL] [Abstract][Full Text] [Related]
19. Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification.
Kamps R; Brandão RD; Bosch BJ; Paulussen AD; Xanthoulea S; Blok MJ; Romano A
Int J Mol Sci; 2017 Jan; 18(2):. PubMed ID: 28146134
[TBL] [Abstract][Full Text] [Related]
20. Simulating Next-Generation Sequencing Datasets from Empirical Mutation and Sequencing Models.
Stephens ZD; Hudson ME; Mainzer LS; Taschuk M; Weber MR; Iyer RK
PLoS One; 2016; 11(11):e0167047. PubMed ID: 27893777
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
