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 *

178 related articles for article (PubMed ID: 36743210)

  • 1. NanoSTR: A method for detection of target short tandem repeats based on nanopore sequencing data.
    Lang J; Xu Z; Wang Y; Sun J; Yang Z
    Front Mol Biosci; 2023; 10():1093519. PubMed ID: 36743210
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Accurate profiling of forensic autosomal STRs using the Oxford Nanopore Technologies MinION device.
    Hall CL; Kesharwani RK; Phillips NR; Planz JV; Sedlazeck FJ; Zascavage RR
    Forensic Sci Int Genet; 2022 Jan; 56():102629. PubMed ID: 34837788
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Forensic nanopore sequencing of STRs and SNPs using Verogen's ForenSeq DNA Signature Prep Kit and MinION.
    Ren ZL; Zhang JR; Zhang XM; Liu X; Lin YF; Bai H; Wang MC; Cheng F; Liu JD; Li P; Kong L; Bo XC; Wang SQ; Ni M; Yan JW
    Int J Legal Med; 2021 Sep; 135(5):1685-1693. PubMed ID: 33950286
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Nanopore sequencing of forensic short tandem repeats using QNome of Qitan Technology.
    Yang TT; Zhang JR; Xie ZH; Ren ZL; Yan JW; Ni M
    Electrophoresis; 2024 Sep; 45(17-18):1535-1545. PubMed ID: 38884206
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Nanopore sequencing of a forensic combined STR and SNP multiplex.
    Tytgat O; Škevin S; Deforce D; Van Nieuwerburgh F
    Forensic Sci Int Genet; 2022 Jan; 56():102621. PubMed ID: 34742095
    [TBL] [Abstract][Full Text] [Related]  

  • 6. WarpSTR: determining tandem repeat lengths using raw nanopore signals.
    Sitarčík J; Vinař T; Brejová B; Krampl W; Budiš J; Radvánszky J; Lucká M
    Bioinformatics; 2023 Jun; 39(6):. PubMed ID: 37326967
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pilot validation of on-field STR typing and human identity testing by MinION nanopore sequencing.
    Luo Y; Zhang J; Ni M; Mei Z; Ye Q; Guo B; Fang L; Feng D; Wang L; Yan J; Wang G
    Electrophoresis; 2024 May; 45(9-10):885-896. PubMed ID: 38356010
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nanopore Sequencing of a Forensic STR Multiplex Reveals Loci Suitable for Single-Contributor STR Profiling.
    Tytgat O; Gansemans Y; Weymaere J; Rubben K; Deforce D; Van Nieuwerburgh F
    Genes (Basel); 2020 Apr; 11(4):. PubMed ID: 32244632
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Accurate typing of short tandem repeats from genome-wide sequencing data and its applications.
    Fungtammasan A; Ananda G; Hile SE; Su MS; Sun C; Harris R; Medvedev P; Eckert K; Makova KD
    Genome Res; 2015 May; 25(5):736-49. PubMed ID: 25823460
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human short tandem repeat identification using a nanopore-based DNA sequencer: a pilot study.
    Asogawa M; Ohno A; Nakagawa S; Ochiai E; Katahira Y; Sudo M; Osawa M; Sugisawa M; Imanishi T
    J Hum Genet; 2020 Jan; 65(1):21-24. PubMed ID: 31649301
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Performance and concordance of the ForenSeq™ system for autosomal and Y chromosome short tandem repeat sequencing of reference-type specimens.
    Just RS; Moreno LI; Smerick JB; Irwin JA
    Forensic Sci Int Genet; 2017 May; 28():1-9. PubMed ID: 28126691
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Profiling of Short-Tandem-Repeat Disease Alleles in 12,632 Human Whole Genomes.
    Tang H; Kirkness EF; Lippert C; Biggs WH; Fabani M; Guzman E; Ramakrishnan S; Lavrenko V; Kakaradov B; Hou C; Hicks B; Heckerman D; Och FJ; Caskey CT; Venter JC; Telenti A
    Am J Hum Genet; 2017 Nov; 101(5):700-715. PubMed ID: 29100084
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Development and validation of a novel 133-plex forensic STR panel (52 STRs and 81 Y-STRs) using single-end 400 bp massive parallel sequencing.
    Fan H; Wang L; Liu C; Lu X; Xu X; Ru K; Qiu P; Liu C; Wen SQ
    Int J Legal Med; 2022 Mar; 136(2):447-464. PubMed ID: 34741666
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic analysis of Southern Brazil subjects using the PowerSeq™ AUTO/Y system for short tandem repeat sequencing.
    Silva DSBS; Sawitzki FR; Scheible MKR; Bailey SF; Alho CS; Faith SA
    Forensic Sci Int Genet; 2018 Mar; 33():129-135. PubMed ID: 29275088
    [TBL] [Abstract][Full Text] [Related]  

  • 15. STRsearch: a new pipeline for targeted profiling of short tandem repeats in massively parallel sequencing data.
    Wang D; Tao R; Li Z; Pan D; Wang Z; Li C; Shi Y
    Hereditas; 2020 Mar; 157(1):8. PubMed ID: 32172688
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of sequence polymorphisms at 58 STRs and 94 iiSNPs in a Tibetan population using massively parallel sequencing.
    Peng D; Zhang Y; Ren H; Li H; Li R; Shen X; Wang N; Huang E; Wu R; Sun H
    Sci Rep; 2020 Jul; 10(1):12225. PubMed ID: 32699278
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Linked-read sequencing for detecting short tandem repeat expansions.
    Chiu R; Rajan-Babu IS; Birol I; Friedman JM
    Sci Rep; 2022 Jun; 12(1):9352. PubMed ID: 35672336
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Short-read, high-throughput sequencing technology for STR genotyping.
    Bornman DM; Hester ME; Schuetter JM; Kasoji MD; Minard-Smith A; Barden CA; Nelson SC; Godbold GD; Baker CH; Yang B; Walther JE; Tornes IE; Yan PS; Rodriguez B; Bundschuh R; Dickens ML; Young BA; Faith SA
    Biotech Rapid Dispatches; 2012 Apr; 2012():1-6. PubMed ID: 25621315
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Filipino DNA variation at 12 X-chromosome short tandem repeat markers.
    Salvador JM; Apaga DLT; Delfin FC; Calacal GC; Dennis SE; De Ungria MCA
    Forensic Sci Int Genet; 2018 Sep; 36():e8-e12. PubMed ID: 29909139
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Developmental validation of the MiSeq FGx Forensic Genomics System for Targeted Next Generation Sequencing in Forensic DNA Casework and Database Laboratories.
    Jäger AC; Alvarez ML; Davis CP; Guzmán E; Han Y; Way L; Walichiewicz P; Silva D; Pham N; Caves G; Bruand J; Schlesinger F; Pond SJK; Varlaro J; Stephens KM; Holt CL
    Forensic Sci Int Genet; 2017 May; 28():52-70. PubMed ID: 28171784
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.