234 related articles for article (PubMed ID: 23065605)
1. Library preparation and data analysis packages for rapid genome sequencing.
Pomraning KR; Smith KM; Bredeweg EL; Connolly LR; Phatale PA; Freitag M
Methods Mol Biol; 2012; 944():1-22. PubMed ID: 23065605
[TBL] [Abstract][Full Text] [Related]
2. Inexpensive multiplexed library preparation for megabase-sized genomes.
Baym M; Kryazhimskiy S; Lieberman TD; Chung H; Desai MM; Kishony R
PLoS One; 2015; 10(5):e0128036. PubMed ID: 26000737
[TBL] [Abstract][Full Text] [Related]
3. Genome analysis of the domestic dog (Korean Jindo) by massively parallel sequencing.
Kim RN; Kim DS; Choi SH; Yoon BH; Kang A; Nam SH; Kim DW; Kim JJ; Ha JH; Toyoda A; Fujiyama A; Kim A; Kim MY; Park KH; Lee KS; Park HS
DNA Res; 2012 Jun; 19(3):275-87. PubMed ID: 22474061
[TBL] [Abstract][Full Text] [Related]
4. SInC: an accurate and fast error-model based simulator for SNPs, Indels and CNVs coupled with a read generator for short-read sequence data.
Pattnaik S; Gupta S; Rao AA; Panda B
BMC Bioinformatics; 2014 Feb; 15():40. PubMed ID: 24495296
[TBL] [Abstract][Full Text] [Related]
5. Combined Genome and Transcriptome (G&T) Sequencing of Single Cells.
Bronner IF; Lorenz S
Methods Mol Biol; 2019; 1979():319-362. PubMed ID: 31028647
[TBL] [Abstract][Full Text] [Related]
6. 96-plex molecular barcoding for the Illumina Genome Analyzer.
Kozarewa I; Turner DJ
Methods Mol Biol; 2011; 733():279-98. PubMed ID: 21431778
[TBL] [Abstract][Full Text] [Related]
7. jackalope: A swift, versatile phylogenomic and high-throughput sequencing simulator.
Nell LA
Mol Ecol Resour; 2020 Jul; 20(4):1132-1140. PubMed ID: 32320523
[TBL] [Abstract][Full Text] [Related]
8. Identification of indels in next-generation sequencing data.
Ratan A; Olson TL; Loughran TP; Miller W
BMC Bioinformatics; 2015 Feb; 16(1):42. PubMed ID: 25879703
[TBL] [Abstract][Full Text] [Related]
9. Sequencing Library Preparation from Degraded Samples for Non-illumina Sequencing Platforms.
Martins RF; Kampmann ML; Förster DW
Methods Mol Biol; 2019; 1963():85-92. PubMed ID: 30875047
[TBL] [Abstract][Full Text] [Related]
10. Preparation of an 8-kb Mate-Pair Library for Illumina Sequencing.
Mardis E; McCombie WR
Cold Spring Harb Protoc; 2017 Apr; 2017(4):pdb.prot094664. PubMed ID: 27803273
[TBL] [Abstract][Full Text] [Related]
11. Optimization of enzymatic fragmentation is crucial to maximize genome coverage: a comparison of library preparation methods for Illumina sequencing.
Ribarska T; Bjørnstad PM; Sundaram AYM; Gilfillan GD
BMC Genomics; 2022 Feb; 23(1):92. PubMed ID: 35105301
[TBL] [Abstract][Full Text] [Related]
12. Next-generation sequencing library construction on a surface.
Feng K; Costa J; Edwards JS
BMC Genomics; 2018 May; 19(1):416. PubMed ID: 29848309
[TBL] [Abstract][Full Text] [Related]
13. SVSR: A Program to Simulate Structural Variations and Generate Sequencing Reads for Multiple Platforms.
Yuan X; Gao M; Bai J; Duan J
IEEE/ACM Trans Comput Biol Bioinform; 2020; 17(3):1082-1091. PubMed ID: 30334804
[TBL] [Abstract][Full Text] [Related]
14. Double-Stranded Library Preparation for Ancient and Other Degraded Samples.
Henneberger K; Barlow A; Paijmans JLA
Methods Mol Biol; 2019; 1963():65-73. PubMed ID: 30875045
[TBL] [Abstract][Full Text] [Related]
15. Multiplexed Illumina sequencing libraries from picogram quantities of DNA.
Bowman SK; Simon MD; Deaton AM; Tolstorukov M; Borowsky ML; Kingston RE
BMC Genomics; 2013 Jul; 14():466. PubMed ID: 23837789
[TBL] [Abstract][Full Text] [Related]
16. Hackflex: low-cost, high-throughput, Illumina Nextera Flex library construction.
Gaio D; Anantanawat K; To J; Liu M; Monahan L; Darling AE
Microb Genom; 2022 Jan; 8(1):. PubMed ID: 35014949
[TBL] [Abstract][Full Text] [Related]
17. Illumina Library Preparation for Sequencing the GC-Rich Fraction of Heterogeneous Genomic DNA.
Tilak MK; Botero-Castro F; Galtier N; Nabholz B
Genome Biol Evol; 2018 Feb; 10(2):616-622. PubMed ID: 29385572
[TBL] [Abstract][Full Text] [Related]
18. Cost-conscious generation of multiplexed short-read DNA libraries for whole-genome sequencing.
Jones A; Stanley D; Ferguson S; Schwessinger B; Borevitz J; Warthmann N
PLoS One; 2023; 18(1):e0280004. PubMed ID: 36706059
[TBL] [Abstract][Full Text] [Related]
19. Genomic Sequence Variation Analysis by Resequencing.
Martin J; Schackwitz W; Lipzen A
Methods Mol Biol; 2018; 1775():229-239. PubMed ID: 29876821
[TBL] [Abstract][Full Text] [Related]
20. Preparation of a 3-kb Mate-Pair Library for Illumina Sequencing.
Mardis E; McCombie WR
Cold Spring Harb Protoc; 2017 Apr; 2017(4):pdb.prot094656. PubMed ID: 27803272
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
