2639 - 2641 |
Novel Applications of Massively Parallel Sequencing (MPS) in Forensic Analysis McCord B, Lee SB |
2642 - 2654 |
Massively parallel sequencing techniques for forensics: A review Bruijns B, Tiggelaar R, Gardeniers H |
2655 - 2668 |
Current state-of-art of STR sequencing in forensic genetics Alonso A, Barrio PA, Muller P, Kocher S, Berger B, Martin P, Bodner M, Willuweit S, Parson W, Roewer L, Budowle B |
2669 - 2673 |
Paternity testing using massively parallel sequencing and the PowerSeq (TM) AUTO/Y system for short tandem repeat sequencing Silva DSBS, Sawitzki FR, Scheible MKR, Bailey SF, Alho CS, Faith SA |
2674 - 2684 |
Evaluation of the performance of Illumina's ForenSeq (TM) system on serially degraded samples Zhang QZ, Zhou Z, Liu QQ, Liu LY, Shao LT, Zhang ML, Ding XR, Gao Y, Wang SQ |
2685 - 2693 |
A closer look at Verogen's Forenseq (TM) DNA Signature Prep kit autosomal and Y-STR data for streamlined analysis of routine reference samples Moreno LI, Galusha MB, Just R |
2694 - 2701 |
Sequence-based US population data for the SE33 locus Borsuk LA, Gettings KB, Steffen CR, Kiesler KM, Vallone PM |
2702 - 2707 |
Massive parallel sequencing of short tandem repeats in the Korean population Kim SY, Lee HC, Chung U, Ham SK, Lee HY, Park SJ, Roh YJ, Lee SH |
2708 - 2724 |
Global patterns of STR sequence variation: Sequencing the CEPH human genome diversity panel for 58 forensic STRs using the Illumina ForenSeq DNA Signature Prep Kit Phillips C, Devesse L, Ballard D, van Weert L, de la Puente M, Melis S, Iglesias VA, Freire-Aradas A, Oldroyd N, Holt C, Court DS, Carracedo A, Lareu MV |
2725 - 2731 |
Development of a massively parallel sequencing assay for investigating sequence polymorphisms of 15 short tandem repeats in a Chinese Northern Han population Zhang QX, Yang M, Pan YJ, Zhao J, Qu BW, Cheng F, Yang YR, Jiao ZP, Liu L, Yan JW |
2732 - 2742 |
Forensic ancestry analysis in two Chinese minority populations using massively parallel sequencing of 165 ancestry-informative SNPs He GL, Wang Z, Wang MG, Luo T, Liu J, Zhou Y, Gao B, Hou YP |
2743 - 2751 |
Development of a SNP panel for predicting biogeographical ancestry and phenotype using massively parallel sequencing Bulbul O, Filoglu G |
2752 - 2756 |
An automated independent workflow for the analysis of massively parallel sequence data from forensic SNP assays Vlachos NT, Meiklejohn KA, Robertson JM |
2757 - 2765 |
Implementing a biogeographic ancestry inference service for forensic casework Jin S, Chase M, Henry M, Alderson G, Morrow JM, Malik S, Ballard D, McGrory J, Fernandopulle N, Millman J, Laird J |
2766 - 2775 |
Sequencing of mitochondrial genomes using the Precision ID mtDNA Whole Genome Panel Pereira V, Longobardi A, Borsting C |
2776 - 2784 |
Performance of the Early Access AmpliSeq (TM) Mitochondrial Panel with degraded DNA samples using the Ion Torrent (TM) platform Wai KT, Barash M, Gunn P |
2785 - 2797 |
Bioinformatic removal of NUMT-associated variants in mitotiling next-generation sequencing data from whole blood samples Ring JD, Sturk-Andreaggi K, Peck MA, Marshall C |
2798 - 2805 |
Evaluation of massively parallel sequencing for forensic DNA methylation profiling Richards R, Patel J, Stevenson K, Harbison S |
2806 - 2814 |
DNA methylation assay based on pyrosequencing for determination of smoking status Alghanim H, Wu WS, McCord B |
2815 - 2823 |
Selecting microhaplotypes optimized for different purposes Kidd KK, Pakstis AJ, Speed WC, Lagace R, Wootton S, Chang J |
2824 - 2832 |
An accurate bacterial DNA quantification assay for HTS library preparation of human biological samples Seashols-Williams S, Green R, Wohlfahrt D, Brand A, Tan-Torres AL, Nogales F, Brooks JP, Singh B |