120 related articles for article (PubMed ID: 28718413)
21. Identification of coding and non-coding mutational hotspots in cancer genomes.
Piraino SW; Furney SJ
BMC Genomics; 2017 Jan; 18(1):17. PubMed ID: 28056774
[TBL] [Abstract][Full Text] [Related]
22. Next generation sequencing reveals genetic landscape of hepatocellular carcinomas.
Li S; Mao M
Cancer Lett; 2013 Nov; 340(2):247-53. PubMed ID: 23063663
[TBL] [Abstract][Full Text] [Related]
23. How evolution of genomes is reflected in exact DNA sequence match statistics.
Massip F; Sheinman M; Schbath S; Arndt PF
Mol Biol Evol; 2015 Feb; 32(2):524-35. PubMed ID: 25398628
[TBL] [Abstract][Full Text] [Related]
24. Somatic mutation in cancer and normal cells.
Martincorena I; Campbell PJ
Science; 2015 Sep; 349(6255):1483-9. PubMed ID: 26404825
[TBL] [Abstract][Full Text] [Related]
25. Cancer genomics: Hard-to-reach repairs.
Khurana E
Nature; 2016 Apr; 532(7598):181-2. PubMed ID: 27075092
[No Abstract] [Full Text] [Related]
26. Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing.
Hoang ML; Kinde I; Tomasetti C; McMahon KW; Rosenquist TA; Grollman AP; Kinzler KW; Vogelstein B; Papadopoulos N
Proc Natl Acad Sci U S A; 2016 Aug; 113(35):9846-51. PubMed ID: 27528664
[TBL] [Abstract][Full Text] [Related]
27. Understanding genomic alterations in cancer genomes using an integrative network approach.
Wang E
Cancer Lett; 2013 Nov; 340(2):261-9. PubMed ID: 23266571
[TBL] [Abstract][Full Text] [Related]
28. Exploring background mutational processes to decipher cancer genetic heterogeneity.
Goncearenco A; Rager SL; Li M; Sang QX; Rogozin IB; Panchenko AR
Nucleic Acids Res; 2017 Jul; 45(W1):W514-W522. PubMed ID: 28472504
[TBL] [Abstract][Full Text] [Related]
29. Differential DNA repair underlies mutation hotspots at active promoters in cancer genomes.
Perera D; Poulos RC; Shah A; Beck D; Pimanda JE; Wong JW
Nature; 2016 Apr; 532(7598):259-63. PubMed ID: 27075100
[TBL] [Abstract][Full Text] [Related]
30. The complex interplay between cell-intrinsic and cell-extrinsic factors driving the evolution of chronic lymphocytic leukemia.
Sutton LA; Rosenquist R
Semin Cancer Biol; 2015 Oct; 34():22-35. PubMed ID: 25963298
[TBL] [Abstract][Full Text] [Related]
31. Predictive genomics: a cancer hallmark network framework for predicting tumor clinical phenotypes using genome sequencing data.
Wang E; Zaman N; Mcgee S; Milanese JS; Masoudi-Nejad A; O'Connor-McCourt M
Semin Cancer Biol; 2015 Feb; 30():4-12. PubMed ID: 24747696
[TBL] [Abstract][Full Text] [Related]
32. Parental influence on human germline de novo mutations in 1,548 trios from Iceland.
Jónsson H; Sulem P; Kehr B; Kristmundsdottir S; Zink F; Hjartarson E; Hardarson MT; Hjorleifsson KE; Eggertsson HP; Gudjonsson SA; Ward LD; Arnadottir GA; Helgason EA; Helgason H; Gylfason A; Jonasdottir A; Jonasdottir A; Rafnar T; Frigge M; Stacey SN; Th Magnusson O; Thorsteinsdottir U; Masson G; Kong A; Halldorsson BV; Helgason A; Gudbjartsson DF; Stefansson K
Nature; 2017 Sep; 549(7673):519-522. PubMed ID: 28959963
[TBL] [Abstract][Full Text] [Related]
33. Population sequencing data reveal a compendium of mutational processes in the human germ line.
Seplyarskiy VB; Soldatov RA; Koch E; McGinty RJ; Goldmann JM; Hernandez RD; Barnes K; Correa A; Burchard EG; Ellinor PT; McGarvey ST; Mitchell BD; Vasan RS; Redline S; Silverman E; Weiss ST; Arnett DK; Blangero J; Boerwinkle E; He J; Montgomery C; Rao DC; Rotter JI; Taylor KD; Brody JA; Chen YI; de Las Fuentes L; Hwu CM; Rich SS; Manichaikul AW; Mychaleckyj JC; Palmer ND; Smith JA; Kardia SLR; Peyser PA; Bielak LF; O'Connor TD; Emery LS; ; ; Gilissen C; Wong WSW; Kharchenko PV; Sunyaev S
Science; 2021 Aug; 373(6558):1030-1035. PubMed ID: 34385354
[TBL] [Abstract][Full Text] [Related]
34. Linking the DNA strand asymmetry to the spatio-temporal replication program. I. About the role of the replication fork polarity in genome evolution.
Baker A; Julienne H; Chen CL; Audit B; d'Aubenton-Carafa Y; Thermes C; Arneodo A
Eur Phys J E Soft Matter; 2012 Sep; 35(9):92. PubMed ID: 23001787
[TBL] [Abstract][Full Text] [Related]
35. Tempo and mode of genomic mutations unveil human evolutionary history.
Hara Y
Genes Genet Syst; 2015; 90(3):123-31. PubMed ID: 26510567
[TBL] [Abstract][Full Text] [Related]
36. From context-dependence of mutations to molecular mechanisms of mutagenesis.
Rogozin IB; Malyarchuk BA; Pavlov YI; Milanesi L
Pac Symp Biocomput; 2005; ():409-20. PubMed ID: 15759646
[TBL] [Abstract][Full Text] [Related]
37. Whole-exome sequencing reveals recurrent somatic mutation networks in cancer.
Liu X; Wang J; Chen L
Cancer Lett; 2013 Nov; 340(2):270-6. PubMed ID: 23153794
[TBL] [Abstract][Full Text] [Related]
38. Yeast evolution and comparative genomics.
Liti G; Louis EJ
Annu Rev Microbiol; 2005; 59():135-53. PubMed ID: 15877535
[TBL] [Abstract][Full Text] [Related]
39. Evolution of the cancer genome.
Yates LR; Campbell PJ
Nat Rev Genet; 2012 Nov; 13(11):795-806. PubMed ID: 23044827
[TBL] [Abstract][Full Text] [Related]
40. Cancer omics: from regulatory networks to clinical outcomes.
Tang B; Hsu PY; Huang TH; Jin VX
Cancer Lett; 2013 Nov; 340(2):277-83. PubMed ID: 23201140
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]