695 related articles for article (PubMed ID: 22228021)
1. Characterizing and interpreting genetic variation from personal genome sequencing.
Johansson AC; Feuk L
Methods Mol Biol; 2012; 838():343-67. PubMed ID: 22228021
[TBL] [Abstract][Full Text] [Related]
2. Detection and interpretation of genomic structural variation in mammals.
Hall IM; Quinlan AR
Methods Mol Biol; 2012; 838():225-48. PubMed ID: 22228015
[TBL] [Abstract][Full Text] [Related]
3. Structural variation analysis with strobe reads.
Ritz A; Bashir A; Raphael BJ
Bioinformatics; 2010 May; 26(10):1291-8. PubMed ID: 20378554
[TBL] [Abstract][Full Text] [Related]
4. Whole genome sequencing.
Ng PC; Kirkness EF
Methods Mol Biol; 2010; 628():215-26. PubMed ID: 20238084
[TBL] [Abstract][Full Text] [Related]
5. The power of NGS technologies to delineate the genome organization in cancer: from mutations to structural variations and epigenetic alterations.
Schweiger MR; Kerick M; Timmermann B; Isau M
Cancer Metastasis Rev; 2011 Jun; 30(2):199-210. PubMed ID: 21267768
[TBL] [Abstract][Full Text] [Related]
6. [Human genome sequencing--next generation technology or will the routine sequencing of human genome be possible?].
Pospísilová S; Tichý B; Mayer J
Cas Lek Cesk; 2009; 148(7):296-302. PubMed ID: 19642294
[TBL] [Abstract][Full Text] [Related]
7. Current state-of-art of sequencing technologies for plant genomics research.
Thudi M; Li Y; Jackson SA; May GD; Varshney RK
Brief Funct Genomics; 2012 Jan; 11(1):3-11. PubMed ID: 22345601
[TBL] [Abstract][Full Text] [Related]
8. Single-molecule DNA sequencing technologies for future genomics research.
Gupta PK
Trends Biotechnol; 2008 Nov; 26(11):602-11. PubMed ID: 18722683
[TBL] [Abstract][Full Text] [Related]
9. Genome variation discovery with high-throughput sequencing data.
Dalca AV; Brudno M
Brief Bioinform; 2010 Jan; 11(1):3-14. PubMed ID: 20053733
[TBL] [Abstract][Full Text] [Related]
10. Application of second-generation sequencing to cancer genomics.
Robison K
Brief Bioinform; 2010 Sep; 11(5):524-34. PubMed ID: 20427421
[TBL] [Abstract][Full Text] [Related]
11. Whole-genome re-sequencing.
Bentley DR
Curr Opin Genet Dev; 2006 Dec; 16(6):545-52. PubMed ID: 17055251
[TBL] [Abstract][Full Text] [Related]
12. [Cancer genome analysis through next-generation sequencing].
Aburatani H
Gan To Kagaku Ryoho; 2011 Jan; 38(1):1-6. PubMed ID: 21368453
[TBL] [Abstract][Full Text] [Related]
13. Genomics. 1000 Genomes Project gives new map of genetic diversity.
Pennisi E
Science; 2010 Oct; 330(6004):574-5. PubMed ID: 21030618
[No Abstract] [Full Text] [Related]
14. Next-generation sequencing technologies for DNA methylation analyses in cancer genomics.
Boerno ST; Grimm C; Lehrach H; Schweiger MR
Epigenomics; 2010 Apr; 2(2):199-207. PubMed ID: 22121870
[TBL] [Abstract][Full Text] [Related]
15. Genome sequencing and assembly.
Grabherr MG; Mauceli E; Ma LJ
Methods Mol Biol; 2011; 722():1-9. PubMed ID: 21590409
[TBL] [Abstract][Full Text] [Related]
16. Guide to the draft human genome.
Wolfsberg TG; McEntyre J; Schuler GD
Nature; 2001 Feb; 409(6822):824-6. PubMed ID: 11236998
[TBL] [Abstract][Full Text] [Related]
17. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
18. Applications of second generation sequencing technologies in complex disorders.
Bayés M; Heath S; Gut IG
Curr Top Behav Neurosci; 2012; 12():321-43. PubMed ID: 22331695
[TBL] [Abstract][Full Text] [Related]
19. Comparative analysis of algorithms for whole-genome assembly of pyrosequencing data.
Finotello F; Lavezzo E; Fontana P; Peruzzo D; Albiero A; Barzon L; Falda M; Di Camillo B; Toppo S
Brief Bioinform; 2012 May; 13(3):269-80. PubMed ID: 22021898
[TBL] [Abstract][Full Text] [Related]
20. Comparison of sequencing based CNV discovery methods using monozygotic twin quartets.
Legault MA; Girard S; Lemieux Perreault LP; Rouleau GA; Dubé MP
PLoS One; 2015; 10(3):e0122287. PubMed ID: 25812131
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
