267 related articles for article (PubMed ID: 26248467)
1. Reducing amplification artifacts in high multiplex amplicon sequencing by using molecular barcodes.
Peng Q; Vijaya Satya R; Lewis M; Randad P; Wang Y
BMC Genomics; 2015 Aug; 16(1):589. PubMed ID: 26248467
[TBL] [Abstract][Full Text] [Related]
2. Generating barcoded libraries for multiplex high-throughput sequencing.
Knapp M; Stiller M; Meyer M
Methods Mol Biol; 2012; 840():155-70. PubMed ID: 22237533
[TBL] [Abstract][Full Text] [Related]
3. Amplification of overlapping DNA amplicons in a single-tube multiplex PCR for targeted next-generation sequencing of BRCA1 and BRCA2.
Schenk D; Song G; Ke Y; Wang Z
PLoS One; 2017; 12(7):e0181062. PubMed ID: 28704513
[TBL] [Abstract][Full Text] [Related]
4. Primer ID Validates Template Sampling Depth and Greatly Reduces the Error Rate of Next-Generation Sequencing of HIV-1 Genomic RNA Populations.
Zhou S; Jones C; Mieczkowski P; Swanstrom R
J Virol; 2015 Aug; 89(16):8540-55. PubMed ID: 26041299
[TBL] [Abstract][Full Text] [Related]
5. Universal and blocking primer mismatches limit the use of high-throughput DNA sequencing for the quantitative metabarcoding of arthropods.
Piñol J; Mir G; Gomez-Polo P; Agustí N
Mol Ecol Resour; 2015 Jul; 15(4):819-30. PubMed ID: 25454249
[TBL] [Abstract][Full Text] [Related]
6. A practical method for barcoding and size-trimming PCR templates for amplicon sequencing.
Mäki A; Rissanen AJ; Tiirola M
Biotechniques; 2016 Feb; 60(2):88-90. PubMed ID: 26842354
[TBL] [Abstract][Full Text] [Related]
7. Sensitive and specific detection of EML4-ALK rearrangements in non-small cell lung cancer (NSCLC) specimens by multiplex amplicon RNA massive parallel sequencing.
Moskalev EA; Frohnauer J; Merkelbach-Bruse S; Schildhaus HU; Dimmler A; Schubert T; Boltze C; König H; Fuchs F; Sirbu H; Rieker RJ; Agaimy A; Hartmann A; Haller F
Lung Cancer; 2014 Jun; 84(3):215-21. PubMed ID: 24674157
[TBL] [Abstract][Full Text] [Related]
8. Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller.
Xu C; Nezami Ranjbar MR; Wu Z; DiCarlo J; Wang Y
BMC Genomics; 2017 Jan; 18(1):5. PubMed ID: 28049435
[TBL] [Abstract][Full Text] [Related]
9. Simple multiplexed PCR-based barcoding of DNA for ultrasensitive mutation detection by next-generation sequencing.
Ståhlberg A; Krzyzanowski PM; Egyud M; Filges S; Stein L; Godfrey TE
Nat Protoc; 2017 Apr; 12(4):664-682. PubMed ID: 28253235
[TBL] [Abstract][Full Text] [Related]
10. Targeting individual cells by barcode in pooled sequence libraries.
Ranu N; Villani AC; Hacohen N; Blainey PC
Nucleic Acids Res; 2019 Jan; 47(1):e4. PubMed ID: 30256981
[TBL] [Abstract][Full Text] [Related]
11. Somatic Mutation Screening Using Archival Formalin-Fixed, Paraffin-Embedded Tissues by Fluidigm Multiplex PCR and Illumina Sequencing.
Wang M; Escudero-Ibarz L; Moody S; Zeng N; Clipson A; Huang Y; Xue X; Grigoropoulos NF; Barrans S; Worrillow L; Forshew T; Su J; Firth A; Martin H; Jack A; Brugger K; Du MQ
J Mol Diagn; 2015 Sep; 17(5):521-32. PubMed ID: 26165823
[TBL] [Abstract][Full Text] [Related]
12. Targeted Single Primer Enrichment Sequencing with Single End Duplex-UMI.
Peng Q; Xu C; Kim D; Lewis M; DiCarlo J; Wang Y
Sci Rep; 2019 Mar; 9(1):4810. PubMed ID: 30886209
[TBL] [Abstract][Full Text] [Related]
13. Targeted RNA-sequencing with competitive multiplex-PCR amplicon libraries.
Blomquist TM; Crawford EL; Lovett JL; Yeo J; Stanoszek LM; Levin A; Li J; Lu M; Shi L; Muldrew K; Willey JC
PLoS One; 2013; 8(11):e79120. PubMed ID: 24236095
[TBL] [Abstract][Full Text] [Related]
14. Multiplex Illumina sequencing using DNA barcoding.
Wong KH; Jin Y; Moqtaderi Z
Curr Protoc Mol Biol; 2013; Chapter 7():Unit 7.11.. PubMed ID: 23288465
[TBL] [Abstract][Full Text] [Related]
15. Collecting in collections: a PCR strategy and primer set for DNA barcoding of decades-old dried museum specimens.
Mitchell A
Mol Ecol Resour; 2015 Sep; 15(5):1102-11. PubMed ID: 25644663
[TBL] [Abstract][Full Text] [Related]
16. Mitigating the effects of reference sequence bias in single-multiplex massively parallel sequencing of the mitochondrial DNA control region.
Huszar TI; Wetton JH; Jobling MA
Forensic Sci Int Genet; 2019 May; 40():9-17. PubMed ID: 30682697
[TBL] [Abstract][Full Text] [Related]
17. Ultrasensitive amplicon barcoding for next-generation sequencing facilitating sequence error and amplification-bias correction.
Ahmed I; Tucci FA; Aflalo A; Smith KGC; Bashford-Rogers RJM
Sci Rep; 2020 Jun; 10(1):10570. PubMed ID: 32601361
[TBL] [Abstract][Full Text] [Related]
18. Accurate multiplexing and filtering for high-throughput amplicon-sequencing.
Esling P; Lejzerowicz F; Pawlowski J
Nucleic Acids Res; 2015 Mar; 43(5):2513-24. PubMed ID: 25690897
[TBL] [Abstract][Full Text] [Related]
19. Multiplex PCR coupled with direct amplicon sequencing for simultaneous detection of numerous waterborne pathogens.
Li B; Saingam P; Ishii S; Yan T
Appl Microbiol Biotechnol; 2019 Jan; 103(2):953-961. PubMed ID: 30417306
[TBL] [Abstract][Full Text] [Related]
20. False positives in multiplex PCR-based next-generation sequencing have unique signatures.
McCall CM; Mosier S; Thiess M; Debeljak M; Pallavajjala A; Beierl K; Deak KL; Datto MB; Gocke CD; Lin MT; Eshleman JR
J Mol Diagn; 2014 Sep; 16(5):541-549. PubMed ID: 25017478
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
