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.
22. Seq-SNPing: multiple-alignment tool for SNP discovery, SNP ID identification, and RFLP genotyping. Chang HW, Chuang LY, Cheng YH, Ho CH, Wen CH, Yang CH. OMICS; 2009 Jun; 13(3):253-60. PubMed ID: 19514837 [Abstract] [Full Text] [Related]
23. Comparison of whole-genome (13X) and capture (87X) resequencing methods for SNP and genotype callings. Roux PF, Marthey S, Djari A, Moroldo M, Esquerré D, Estellé J, Klopp C, Lagarrigue S, Demeure O. Anim Genet; 2015 Feb; 46(1):82-6. PubMed ID: 25515399 [Abstract] [Full Text] [Related]
24. High performance DNA sequencing, and the detection of mutations and polymorphisms, on the Clipper sequencer. Yager TD, Baron L, Batra R, Bouevitch A, Chan D, Chan K, Darasch S, Gilchrist R, Izmailov A, Lacroix JM, Marchelleta K, Renfrew J, Renfrew J, Rushlow D, Steinbach E, Ton C, Waterhouse P, Zaleski H, Dunn JM, Stevens J. Electrophoresis; 1999 Jun; 20(6):1280-300. PubMed ID: 10380769 [Abstract] [Full Text] [Related]
25. Large scale sequencing. Stein L. Curr Protoc Bioinformatics; 2003 Aug; Chapter 11():Unit11.1. PubMed ID: 18428694 [Abstract] [Full Text] [Related]
28. Fluorescence resonance energy transfer dye nucleotide terminators: a new synthetic approach for high-throughout DNA sequencing. Nampalli S, Khot M, Nelson JR, Flick PK, Fuller CW, Kumar S. Nucleosides Nucleotides Nucleic Acids; 2001 Aug; 20(4-7):361-7. PubMed ID: 11563048 [Abstract] [Full Text] [Related]
31. SeqDoC: rapid SNP and mutation detection by direct comparison of DNA sequence chromatograms. Crowe ML. BMC Bioinformatics; 2005 May 31; 6():133. PubMed ID: 15927052 [Abstract] [Full Text] [Related]
34. Fluorescent microsphere-based readout technology for multiplexed human single nucleotide polymorphism analysis and bacterial identification. Ye F, Li MS, Taylor JD, Nguyen Q, Colton HM, Casey WM, Wagner M, Weiner MP, Chen J. Hum Mutat; 2001 Apr 31; 17(4):305-16. PubMed ID: 11295829 [Abstract] [Full Text] [Related]
35. DMSO resolves certain compressions and signal dropouts in fluorescent dye labeled primer-based DNA sequencing reactions. Seto D, Seto J, Deshpande P, Hood L. DNA Seq; 1995 Apr 31; 5(3):131-40. PubMed ID: 7612923 [Abstract] [Full Text] [Related]
37. Quantitative detection of HIV-1 drug resistance mutations by automated DNA sequencing. Larder BA, Kohli A, Kellam P, Kemp SD, Kronick M, Henfrey RD. Nature; 1993 Oct 14; 365(6447):671-3. PubMed ID: 8413632 [Abstract] [Full Text] [Related]
38. Producing STR locus patterns from bloodstains and other forensic samples using an infrared fluorescent automated DNA sequencer. Roy R, Steffens DL, Gartside B, Jang GY, Brumbaugh JA. J Forensic Sci; 1996 May 14; 41(3):418-24. PubMed ID: 8656180 [Abstract] [Full Text] [Related]