Identification of single nucleotide variants using position-specific error estimation in deep sequencing data

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1755-8794

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Identification of single nucleotide variants using position-specific error estimation in deep sequencing data ; volume:12 ; number:1 ; day:2 ; month:8 ; year:2019 ; pages:1-12 ; date:12.2019
BMC medical genomics ; 12, Heft 1 (2.8.2019), 1-12, 12.2019

Creator: Kleftogiannis, Dimitrios
Punta, Marco
Jayaram, Anuradha
Sandhu, Shahneen
Wong, Stephen Q.
Gasi Tandefelt, Delila
Conteduca, Vincenza
Wetterskog, Daniel
Attard, Gerhardt
Lise, Stefano

Contributor: SpringerLink (Online service)

DOI: 10.1186/s12920-019-0557-9

URN: urn:nbn:de:101:1-2019122700040498123929

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

Last update: 14.08.2025, 10:57 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

Kleftogiannis, Dimitrios
Punta, Marco
Jayaram, Anuradha
Sandhu, Shahneen
Wong, Stephen Q.
Gasi Tandefelt, Delila
Conteduca, Vincenza
Wetterskog, Daniel
Attard, Gerhardt
Lise, Stefano
SpringerLink (Online service)

Other Objects (12)

SNVHMM: predicting single nucleotide variants from next generation sequencing

Global inference of disease-causing single nucleotide variants from exome sequencing data

Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing

The discrepancy among single nucleotide variants detected by DNA and RNA high throughput sequencing data

SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing data

A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

Echoed induction of nucleotide variants and chromosomal structural variants in cancer cells

Whole-genome sequencing of artificial single-nucleotide variants induced by DNA degradation in biological crime scene traces

Discovering nucleotide-level and structural variants in cancer genome data from second- and third-generation sequencing technologies

Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

Collective judgment predicts disease-associated single nucleotide variants

Estimating sequencing error rates using families

SNVHMM: predicting single nucleotide variants from next generation sequencing

Global inference of disease-causing single nucleotide variants from exome sequencing data

Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing

The discrepancy among single nucleotide variants detected by DNA and RNA high throughput sequencing data

SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing data

A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

Echoed induction of nucleotide variants and chromosomal structural variants in cancer cells

Whole-genome sequencing of artificial single-nucleotide variants induced by DNA degradation in biological crime scene traces

Discovering nucleotide-level and structural variants in cancer genome data from second- and third-generation sequencing technologies

Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

Collective judgment predicts disease-associated single nucleotide variants

Estimating sequencing error rates using families

SNVHMM: predicting single nucleotide variants from next generation sequencing

Global inference of disease-causing single nucleotide variants from exome sequencing data

Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing

The discrepancy among single nucleotide variants detected by DNA and RNA high throughput sequencing data

SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing data

A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

Echoed induction of nucleotide variants and chromosomal structural variants in cancer cells

Whole-genome sequencing of artificial single-nucleotide variants induced by DNA degradation in biological crime scene traces

Discovering nucleotide-level and structural variants in cancer genome data from second- and third-generation sequencing technologies

Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

Collective judgment predicts disease-associated single nucleotide variants

Estimating sequencing error rates using families

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.

Identification of single nucleotide variants using position-specific error estimation in deep sequencing data

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

SNVHMM: predicting single nucleotide variants from next generation sequencing

Global inference of disease-causing single nucleotide variants from exome sequencing data

Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing

The discrepancy among single nucleotide variants detected by DNA and RNA high throughput sequencing data

SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing data

A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

Echoed induction of nucleotide variants and chromosomal structural variants in cancer cells

Whole-genome sequencing of artificial single-nucleotide variants induced by DNA degradation in biological crime scene traces

Discovering nucleotide-level and structural variants in cancer genome data from second- and third-generation sequencing technologies

Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

Collective judgment predicts disease-associated single nucleotide variants

Estimating sequencing error rates using families

SNVHMM: predicting single nucleotide variants from next generation sequencing

Global inference of disease-causing single nucleotide variants from exome sequencing data

Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing

The discrepancy among single nucleotide variants detected by DNA and RNA high throughput sequencing data

SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing data

A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

Echoed induction of nucleotide variants and chromosomal structural variants in cancer cells

Whole-genome sequencing of artificial single-nucleotide variants induced by DNA degradation in biological crime scene traces

Discovering nucleotide-level and structural variants in cancer genome data from second- and third-generation sequencing technologies

Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

Collective judgment predicts disease-associated single nucleotide variants

Estimating sequencing error rates using families

SNVHMM: predicting single nucleotide variants from next generation sequencing

Global inference of disease-causing single nucleotide variants from exome sequencing data

Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing

The discrepancy among single nucleotide variants detected by DNA and RNA high throughput sequencing data

SIEVE: joint inference of single-nucleotide variants and cell phylogeny from single-cell DNA sequencing data

A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

Echoed induction of nucleotide variants and chromosomal structural variants in cancer cells

Whole-genome sequencing of artificial single-nucleotide variants induced by DNA degradation in biological crime scene traces

Discovering nucleotide-level and structural variants in cancer genome data from second- and third-generation sequencing technologies

Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

Collective judgment predicts disease-associated single nucleotide variants

Estimating sequencing error rates using families

Related objects

Reset password