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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

327 related items for PubMed ID: 30101986

  • 21.
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  • 22. 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, Álvarez Iglesias V, Freire-Aradas A, Oldroyd N, Holt C, Syndercombe Court D, Carracedo Á, Lareu MV.
    Electrophoresis; 2018 Nov; 39(21):2708-2724. PubMed ID: 30101987
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  • 24. Introduction of the Python script STRinNGS for analysis of STR regions in FASTQ or BAM files and expansion of the Danish STR sequence database to 11 STRs.
    Friis SL, Buchard A, Rockenbauer E, Børsting C, Morling N.
    Forensic Sci Int Genet; 2016 Mar; 21():68-75. PubMed ID: 26722765
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  • 27. Progress in the implementation of massively parallel sequencing for forensic genetics: results of a European-wide survey among professional users.
    Gross TE, Fleckhaus J, Schneider PM.
    Int J Legal Med; 2021 Jul; 135(4):1425-1432. PubMed ID: 33847802
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  • 28. A closer look at Verogen's Forenseq™ DNA Signature Prep kit autosomal and Y-STR data for streamlined analysis of routine reference samples.
    Moreno LI, Galusha MB, Just R.
    Electrophoresis; 2018 Nov; 39(21):2685-2693. PubMed ID: 30025170
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  • 29. Capture enrichment and massively parallel sequencing for human identification.
    Gorden EM, Sturk-Andreaggi K, Marshall C.
    Forensic Sci Int Genet; 2021 Jul; 53():102496. PubMed ID: 33770700
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  • 30. Improved STR analysis of degraded DNA from human skeletal remains through in-house MPS-STR panel.
    Cho S, Shin KJ, Bae SJ, Kwon YL, Lee SD.
    Electrophoresis; 2020 Oct; 41(18-19):1600-1605. PubMed ID: 32725901
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  • 31. Massively parallel sequencing of 25 short tandem repeat loci including the SE33 marker in Koreans.
    Lee JH, Kim J, Kim H, Kim HS, Kim E.
    Genes Genomics; 2021 Feb; 43(2):133-140. PubMed ID: 33481226
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  • 34. Parallel sequencing of 87 STR and 294 SNP markers using the prototype of the SifaMPS panel on the MiSeq FGx™ system.
    Tao R, Wang S, Chen A, Xia R, Zhang X, Yang Q, Qu Y, Zhang S, Li C.
    Forensic Sci Int Genet; 2021 May; 52():102490. PubMed ID: 33689955
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  • 35. Optimizing DNA recovery and forensic typing of degraded blood and dental remains using a specialized extraction method, comprehensive qPCR sample characterization, and massively parallel sequencing.
    Carrasco P, Inostroza C, Didier M, Godoy M, Holt CL, Tabak J, Loftus A.
    Int J Legal Med; 2020 Jan; 134(1):79-91. PubMed ID: 31414202
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  • 36. Analysis of complex DNA mixtures using massively parallel sequencing of SNPs with low minor allele frequencies.
    Petrovick MS, Boettcher T, Fremont-Smith P, Peragallo C, Ricke DO, Watkins J, Schwoebel E.
    Forensic Sci Int Genet; 2020 May; 46():102234. PubMed ID: 32018060
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  • 38. Massively parallel sequencing of 32 forensic markers using the Precision ID GlobalFiler™ NGS STR Panel and the Ion PGM™ System.
    Wang Z, Zhou D, Wang H, Jia Z, Liu J, Qian X, Li C, Hou Y.
    Forensic Sci Int Genet; 2017 Nov; 31():126-134. PubMed ID: 28938153
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  • 39. Developmental validation of the ForenSeq MainstAY kit, MiSeq FGx sequencing system and ForenSeq Universal Analysis Software.
    Stephens KM, Barta R, Fleming K, Perez JC, Wu SF, Snedecor J, Holt CL, LaRue B, Budowle B.
    Forensic Sci Int Genet; 2023 May; 64():102851. PubMed ID: 36907074
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  • 40. Paternity testing using massively parallel sequencing and the PowerSeq™ AUTO/Y system for short tandem repeat sequencing.
    S B S Silva D, Sawitzki FR, Scheible MKR, Bailey SF, S Alho C, Faith SA.
    Electrophoresis; 2018 Nov; 39(21):2669-2673. PubMed ID: 30132945
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