[HTML][HTML] Combining callers improves the detection of copy number variants from whole-genome sequencing
Abstract Copy Number Variants (CNVs) are deletions, duplications or insertions larger than
50 base pairs. They account for a large percentage of the normal genome variation and play …
50 base pairs. They account for a large percentage of the normal genome variation and play …
Combining callers improves the detection of copy number variants from whole-genome sequencing
M Coutelier, M Holtgrewe, M Jäger… - European Journal of …, 2022 - edoc.mdc-berlin.de
Copy Number Variants (CNVs) are deletions, duplications or insertions larger than 50 base
pairs. They account for a large percentage of the normal genome variation and play major …
pairs. They account for a large percentage of the normal genome variation and play major …
[HTML][HTML] Combining callers improves the detection of copy number variants from whole-genome sequencing
M Coutelier, M Holtgrewe, M Jäger… - European Journal of …, 2022 - ncbi.nlm.nih.gov
Abstract Copy Number Variants (CNVs) are deletions, duplications or insertions larger than
50 base pairs. They account for a large percentage of the normal genome variation and play …
50 base pairs. They account for a large percentage of the normal genome variation and play …
Combining callers improves the detection of copy number variants from whole-genome sequencing.
M Coutelier, M Holtgrewe, M Jäger… - European Journal of …, 2021 - europepmc.org
Abstract Copy Number Variants (CNVs) are deletions, duplications or insertions larger than
50 base pairs. They account for a large percentage of the normal genome variation and play …
50 base pairs. They account for a large percentage of the normal genome variation and play …
Combining callers improves the detection of copy number variants from whole-genome sequencing
M Coutelier, M Holtgrewe, M Jäger… - … Journal of Human …, 2021 - refubium.fu-berlin.de
Copy Number Variants (CNVs) are deletions, duplications or insertions larger than 50 base
pairs. They account for a large percentage of the normal genome variation and play major …
pairs. They account for a large percentage of the normal genome variation and play major …
Combining callers improves the detection of copy number variants from whole-genome sequencing
M Coutelier, M Holtgrewe, M Jäger… - … journal of human …, 2022 - pubmed.ncbi.nlm.nih.gov
Copy Number Variants (CNVs) are deletions, duplications or insertions larger than 50 base
pairs. They account for a large percentage of the normal genome variation and play major …
pairs. They account for a large percentage of the normal genome variation and play major …
Combining callers improves the detection of copy number variants from whole-genome sequencing.
M Coutelier, M Holtgrewe, M Jäger… - European Journal of …, 2021 - europepmc.org
Abstract Copy Number Variants (CNVs) are deletions, duplications or insertions larger than
50 base pairs. They account for a large percentage of the normal genome variation and play …
50 base pairs. They account for a large percentage of the normal genome variation and play …
Combining callers improves the detection of copy number variants from whole-genome sequencing
M Coutelier, M Holtgrewe, M Jäger… - European Journal of …, 2022 - edoc.mdc-berlin.de
Copy Number Variants (CNVs) are deletions, duplications or insertions larger than 50 base
pairs. They account for a large percentage of the normal genome variation and play major …
pairs. They account for a large percentage of the normal genome variation and play major …