Add to ORKGNon-synonymous variations in cancer and their effects on the human pro rare and novel SNVs that are not present in dbSNP and therefore provides a more comprehensive understanding of Cole et al. BMC Bioinformatics 2014, 15:2
rti ce e ev informatics resource that has transformed the analysis of cancer or autism [13-16]. Hill...
Background: Systematic approaches for identifying proteins involved in different types of cancer are...
Excitement and controversy followed the discovery that a frequently occurring single nucleotide poly...
International audienceSingle-nucleotide variants (SNVs) are the most frequent genetic changes found ...
are Rare): methods to facilitate the analysis of iants from massively publication identifying XRCC2 ...
Background: Identifying similarities and differences in the molecular constitutions of various types...
Development of high-throughput monitoring technologies enables interrogation of cancer samples at va...
ar nt is one of the main challenges in functional genomics and In particular, DE analysis is a widel...
, RI 02912, USA Full list of author information is available at the end of the article the problem o...
nn at3 Background A number of preclinical studies have demonstrated that Schem et al. BMC Cancer 201...
Identifying cancer mutation targets across thousands of samples: MuteProc, a high throughput mutatio...
This is an Accepted Manuscript of an article published by Taylor & Francis in Expert Review of Molec...
An amendment to this paper has been published and can be accessed via a link at the top of the paper...
Cancer is a heterogeneous disease, which is comprised of a collection of diseases traditionally cate...
Contains fulltext : 137464.pdf (publisher's version ) (Closed access)Head and neck...
rti ce e ev informatics resource that has transformed the analysis of cancer or autism [13-16]. Hill...
Background: Systematic approaches for identifying proteins involved in different types of cancer are...
Excitement and controversy followed the discovery that a frequently occurring single nucleotide poly...
International audienceSingle-nucleotide variants (SNVs) are the most frequent genetic changes found ...
are Rare): methods to facilitate the analysis of iants from massively publication identifying XRCC2 ...
Background: Identifying similarities and differences in the molecular constitutions of various types...
Development of high-throughput monitoring technologies enables interrogation of cancer samples at va...
ar nt is one of the main challenges in functional genomics and In particular, DE analysis is a widel...
, RI 02912, USA Full list of author information is available at the end of the article the problem o...
nn at3 Background A number of preclinical studies have demonstrated that Schem et al. BMC Cancer 201...
Identifying cancer mutation targets across thousands of samples: MuteProc, a high throughput mutatio...
This is an Accepted Manuscript of an article published by Taylor & Francis in Expert Review of Molec...
An amendment to this paper has been published and can be accessed via a link at the top of the paper...
Cancer is a heterogeneous disease, which is comprised of a collection of diseases traditionally cate...
Contains fulltext : 137464.pdf (publisher's version ) (Closed access)Head and neck...
rti ce e ev informatics resource that has transformed the analysis of cancer or autism [13-16]. Hill...
Background: Systematic approaches for identifying proteins involved in different types of cancer are...
Excitement and controversy followed the discovery that a frequently occurring single nucleotide poly...