Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 290

1.

Opportunities and methods for studying alternative splicing in cancer with RNA-Seq.

Feng H, Qin Z, Zhang X.

Cancer Lett. 2013 Nov 1;340(2):179-91. doi: 10.1016/j.canlet.2012.11.010. Epub 2012 Nov 27. Review.

PMID:
23196057
2.

Next-generation sequencing in the clinic: promises and challenges.

Xuan J, Yu Y, Qing T, Guo L, Shi L.

Cancer Lett. 2013 Nov 1;340(2):284-95. doi: 10.1016/j.canlet.2012.11.025. Epub 2012 Nov 19. Review.

PMID:
23174106
3.

Beyond microRNA--novel RNAs derived from small non-coding RNA and their implication in cancer.

Martens-Uzunova ES, Olvedy M, Jenster G.

Cancer Lett. 2013 Nov 1;340(2):201-11. doi: 10.1016/j.canlet.2012.11.058. Epub 2013 Jan 29. Review.

4.

Next generation sequencing applications in cancer research.

Zhang W, Nykter M, Chen K.

Cancer Lett. 2013 Nov 1;340(2):149-50. doi: 10.1016/j.canlet.2013.05.026. Epub 2013 Jun 11. No abstract available.

PMID:
23764479
5.

Cancer omics: from regulatory networks to clinical outcomes.

Tang B, Hsu PY, Huang TH, Jin VX.

Cancer Lett. 2013 Nov 1;340(2):277-83. doi: 10.1016/j.canlet.2012.11.033. Epub 2012 Nov 29. Review.

PMID:
23201140
6.

Cancer heterogeneity and "the struggle for existence": diagnostic and analytical challenges.

Horswell S, Matthews N, Swanton C.

Cancer Lett. 2013 Nov 1;340(2):220-6. doi: 10.1016/j.canlet.2012.10.031. Epub 2012 Nov 8. Review.

PMID:
23142290
7.

Understanding genomic alterations in cancer genomes using an integrative network approach.

Wang E.

Cancer Lett. 2013 Nov 1;340(2):261-9. doi: 10.1016/j.canlet.2012.11.050. Epub 2012 Dec 22. Review.

PMID:
23266571
8.

Sequencing the transcriptional network of androgen receptor in prostate cancer.

Chng KR, Cheung E.

Cancer Lett. 2013 Nov 1;340(2):254-60. doi: 10.1016/j.canlet.2012.11.009. Epub 2012 Nov 27. Review.

PMID:
23196061
9.

Whole-exome sequencing reveals recurrent somatic mutation networks in cancer.

Liu X, Wang J, Chen L.

Cancer Lett. 2013 Nov 1;340(2):270-6. doi: 10.1016/j.canlet.2012.11.002. Epub 2012 Nov 12. Review.

PMID:
23153794
10.

Next generation sequencing reveals genetic landscape of hepatocellular carcinomas.

Li S, Mao M.

Cancer Lett. 2013 Nov 1;340(2):247-53. doi: 10.1016/j.canlet.2012.09.027. Epub 2012 Oct 12. Review.

PMID:
23063663
11.

Next-generation biobanking of metastases to enable multidimensional molecular profiling in personalized medicine.

Diaz Z, Aguilar-Mahecha A, Paquet ER, Basik M, Orain M, Camlioglu E, Constantin A, Benlimame N, Bachvarov D, Jannot G, Simard MJ, Chabot B, Gologan A, Klinck R, Gagnon-Kugler T, Lespérance B, Samson B, Kavan P, Alcindor T, Dalfen R, Lan C, Chabot C, Buchanan M, Przybytkowski E, Qureshi S, Rousseau C, Spatz A, Têtu B, Batist G.

Mod Pathol. 2013 Nov;26(11):1413-24. doi: 10.1038/modpathol.2013.81. Epub 2013 Jun 7.

12.

Comprehensive genome sequencing of the liver cancer genome.

Nakagawa H, Shibata T.

Cancer Lett. 2013 Nov 1;340(2):234-40. doi: 10.1016/j.canlet.2012.10.035. Epub 2012 Nov 8. Review.

PMID:
23142287
13.

Analyzing the cancer methylome through targeted bisulfite sequencing.

Lee EJ, Luo J, Wilson JM, Shi H.

Cancer Lett. 2013 Nov 1;340(2):171-8. doi: 10.1016/j.canlet.2012.10.040. Epub 2012 Nov 28. Review.

14.

Identifying differential alternative splicing events from RNA sequencing data using RNASeq-MATS.

Park JW, Tokheim C, Shen S, Xing Y.

Methods Mol Biol. 2013;1038:171-9. doi: 10.1007/978-1-62703-514-9_10.

PMID:
23872975
15.

RNA-Seq for transcriptome analysis in non-model plants.

Garg R, Jain M.

Methods Mol Biol. 2013;1069:43-58. doi: 10.1007/978-1-62703-613-9_4.

PMID:
23996307
16.

SplicingCompass: differential splicing detection using RNA-seq data.

Aschoff M, Hotz-Wagenblatt A, Glatting KH, Fischer M, Eils R, König R.

Bioinformatics. 2013 May 1;29(9):1141-8. doi: 10.1093/bioinformatics/btt101. Epub 2013 Feb 28.

PMID:
23449093
17.

Cancer genome sequencing: understanding malignancy as a disease of the genome, its conformation, and its evolution.

Patel LR, Nykter M, Chen K, Zhang W.

Cancer Lett. 2013 Nov 1;340(2):152-60. doi: 10.1016/j.canlet.2012.10.018. Epub 2012 Oct 27. Review.

18.

Genomic sequencing in cancer.

Tuna M, Amos CI.

Cancer Lett. 2013 Nov 1;340(2):161-70. doi: 10.1016/j.canlet.2012.11.004. Epub 2012 Nov 23. Review.

19.

Fusion genes and their discovery using high throughput sequencing.

Annala MJ, Parker BC, Zhang W, Nykter M.

Cancer Lett. 2013 Nov 1;340(2):192-200. doi: 10.1016/j.canlet.2013.01.011. Epub 2013 Jan 29. Review.

20.

Splice variants as cancer biomarkers.

Brinkman BM.

Clin Biochem. 2004 Jul;37(7):584-94. Review.

PMID:
15234240

Supplemental Content

Support Center