OmicsDI
Toggle navigation
Browse
Submit Data
Databases
API
Help
Advanced
Search
19
Results
Show all
Save search
Copy query
Show results for
Unknown
(19)
Publication Date
Release Date
2020
(16)
2022
(2)
2025
(1)
Previous
page
1 / 2
You're on page
1
page
2
Next
page
Sort
by:
Relevance
Page size
10
Assessing reproducibility of inherited variants detected with short-read whole genome sequencing.
Not available
S-EPMC8722114
|
biostudies-literature
Cite
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples.
Not available
S-EPMC7505971
|
biostudies-literature
Cite
Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig.
Not available
S-EPMC7002414
|
biostudies-literature
Cite
Inferring structural variant cancer cell fraction.
Not available
S-EPMC7002525
|
biostudies-literature
Cite
The landscape of viral associations in human cancers.
Not available
S-EPMC8076016
|
biostudies-literature
Cite
Divergent mutational processes distinguish hypoxic and normoxic tumours.
Not available
S-EPMC7002770
|
biostudies-literature
Cite
Comprehensive molecular characterization of mitochondrial genomes in human cancers.
Not available
S-EPMC7058535
|
biostudies-literature
Cite
Pan-cancer analysis of whole genomes.
Not available
S-EPMC7025898
|
biostudies-literature
Cite
Combined burden and functional impact tests for cancer driver discovery using DriverPower.
Not available
S-EPMC7002750
|
biostudies-literature
Cite
Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis.
Not available
S-EPMC7002399
|
biostudies-literature
Cite
Previous
page
1 / 2
You're on page
1
page
2
Next
page
Sort
by:
Relevance
Page size
10
OmicsDI
is part of the ELIXIR infrastructure
OmicsDI is an Elixir interoperability service.
Learn more ›
Tweets