Correction: Improving somatic exome sequencing performance by biological replicates

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Correction: Improving somatic exome sequencing performance by biological replicates ; volume:25 ; number:1 ; day:25 ; month:6 ; year:2024 ; pages:1 ; date:12.2024
BMC bioinformatics ; 25, Heft 1 (25.6.2024), 1, 12.2024

Creator: Cebeci, Yunus Emre
Erturk, Rumeysa Aslihan
Ergun, Mehmet Arif
Baysan, Mehmet

Contributor: SpringerLink (Online service)

DOI: 10.1186/s12859-024-05828-0

URN: urn:nbn:de:101:1-2409152104581.813421119953

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 18.08.3025, 3:18 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Cebeci, Yunus Emre
Erturk, Rumeysa Aslihan
Ergun, Mehmet Arif
Baysan, Mehmet
SpringerLink (Online service)

Other Objects (12)

Improving somatic exome sequencing performance by biological replicates

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Improving somatic variant identification through integration of genome and exome data

Whole exome sequencing reveals novel somatic alterations in neuroblastoma patients with chemotherapy

Somatic mutational landscape across Indian breast cancer cases by whole exome sequencing

Exome sequencing identifies novel somatic variants in African American esophageal squamous cell carcinoma

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Somatic mutations in renal cell carcinomas from Chinese patients revealed by whole exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia

SNES: single nucleus exome sequencing

Exome sequencing in hereditary nephropathies

Improving somatic exome sequencing performance by biological replicates

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Improving somatic variant identification through integration of genome and exome data

Whole exome sequencing reveals novel somatic alterations in neuroblastoma patients with chemotherapy

Somatic mutational landscape across Indian breast cancer cases by whole exome sequencing

Exome sequencing identifies novel somatic variants in African American esophageal squamous cell carcinoma

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Somatic mutations in renal cell carcinomas from Chinese patients revealed by whole exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia

SNES: single nucleus exome sequencing

Exome sequencing in hereditary nephropathies

Improving somatic exome sequencing performance by biological replicates

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Improving somatic variant identification through integration of genome and exome data

Whole exome sequencing reveals novel somatic alterations in neuroblastoma patients with chemotherapy

Somatic mutational landscape across Indian breast cancer cases by whole exome sequencing

Exome sequencing identifies novel somatic variants in African American esophageal squamous cell carcinoma

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Somatic mutations in renal cell carcinomas from Chinese patients revealed by whole exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia

SNES: single nucleus exome sequencing

Exome sequencing in hereditary nephropathies

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Correction: Improving somatic exome sequencing performance by biological replicates

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Improving somatic exome sequencing performance by biological replicates

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Improving somatic variant identification through integration of genome and exome data

Whole exome sequencing reveals novel somatic alterations in neuroblastoma patients with chemotherapy

Somatic mutational landscape across Indian breast cancer cases by whole exome sequencing

Exome sequencing identifies novel somatic variants in African American esophageal squamous cell carcinoma

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Somatic mutations in renal cell carcinomas from Chinese patients revealed by whole exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia

SNES: single nucleus exome sequencing

Exome sequencing in hereditary nephropathies

Improving somatic exome sequencing performance by biological replicates

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Improving somatic variant identification through integration of genome and exome data

Whole exome sequencing reveals novel somatic alterations in neuroblastoma patients with chemotherapy

Somatic mutational landscape across Indian breast cancer cases by whole exome sequencing

Exome sequencing identifies novel somatic variants in African American esophageal squamous cell carcinoma

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Somatic mutations in renal cell carcinomas from Chinese patients revealed by whole exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia

SNES: single nucleus exome sequencing

Exome sequencing in hereditary nephropathies

Improving somatic exome sequencing performance by biological replicates

Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples

Improving somatic variant identification through integration of genome and exome data

Whole exome sequencing reveals novel somatic alterations in neuroblastoma patients with chemotherapy

Somatic mutational landscape across Indian breast cancer cases by whole exome sequencing

Exome sequencing identifies novel somatic variants in African American esophageal squamous cell carcinoma

Intersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers

Somatic mutations in renal cell carcinomas from Chinese patients revealed by whole exome sequencing

Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia

SNES: single nucleus exome sequencing

Exome sequencing in hereditary nephropathies

Related objects

Reset password