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1.
smCounter2: an accurate low-frequency variant caller for targeted sequencing data with unique molecular identifiers.
Bioinformatics
; 35(8): 1299-1309, 2019 04 15.
Article
in English
| MEDLINE | ID: mdl-30192920
2.
Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer.
JAMA
; 319(23): 2401-2409, 2018 06 19.
Article
in English
| MEDLINE | ID: mdl-29922827
3.
Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller.
BMC Genomics
; 18(1): 5, 2017 01 03.
Article
in English
| MEDLINE | ID: mdl-28049435
4.
Quantitative analysis of differences in copy numbers using read depth obtained from PCR-enriched samples and controls.
BMC Bioinformatics
; 16: 17, 2015 Jan 28.
Article
in English
| MEDLINE | ID: mdl-25626454
5.
Edge effects in calling variants from targeted amplicon sequencing.
BMC Genomics
; 15: 1073, 2014 Dec 05.
Article
in English
| MEDLINE | ID: mdl-25480444
6.
Comparison of somatic mutation calling methods in amplicon and whole exome sequence data.
BMC Genomics
; 15: 244, 2014 Mar 28.
Article
in English
| MEDLINE | ID: mdl-24678773
7.
Development of a Smart Sleep Mask with Multiple Sensors.
Annu Int Conf IEEE Eng Med Biol Soc
; 2021: 7058-7062, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34892728
8.
Targeted Single Primer Enrichment Sequencing with Single End Duplex-UMI.
Sci Rep
; 9(1): 4810, 2019 03 18.
Article
in English
| MEDLINE | ID: mdl-30886209
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