Fast and Easy Nanopore Sequencing Workflow for Rapid Genetic Testing of Familial Hypercholesterolemia
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
In: 10.3389/fgene.2022.836231
- Ereignis
-
Veröffentlichung
- (wo)
-
Marburg
- (wer)
-
Philipps-Universität Marburg
- (wann)
-
2022
- Urheber
-
Souf, Muhidien
Bedenbender, Simon
Ruppert, Volker
Kurt, Bilgen
Schieffer, Bernhard
Schaefer, Juergen R.
- URN
-
urn:nbn:de:hebis:04-es2022-01413
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:41 MEZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Souf, Muhidien
- Bedenbender, Simon
- Ruppert, Volker
- Kurt, Bilgen
- Schieffer, Bernhard
- Schaefer, Juergen R.
- Philipps-Universität Marburg
Entstanden
- 2022
Ähnliche Objekte (12)
Rapid Diagnosis of Familial Defective Apolipoprotein B-100
poreCov-An Easy to Use, Fast, and Robust Workflow for SARS-CoV-2 Genome Reconstruction via Nanopore Sequencing
Rapid identification of ENU mutations by high-throughput sequencing
Familial Feeling
Whole-exome sequencing identifies a novel germline variant in PTK7 gene in familial colorectal cancer
Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma [Letter]
Whole exome sequencing identifies APCDD1 and HDAC5 genes as potentially cancer predisposing in familial colorectal cancer
Familial chylomicronemia syndrome
Customized workflow development and data modularization concepts for RNA-Sequencing and metatranscriptome experiments
Monitoring rapid evolution of plant populations at scale with pool-sequencing
Genotyping of familial Mediterranean fever gene (MEFV)—Single nucleotide polymorphism—Comparison of Nanopore with conventional Sanger sequencing
Optimized and affordable high‐throughput sequencing workflow for preserved and nonpreserved small zooplankton specimens
Rapid Diagnosis of Familial Defective Apolipoprotein B-100
poreCov-An Easy to Use, Fast, and Robust Workflow for SARS-CoV-2 Genome Reconstruction via Nanopore Sequencing
Rapid identification of ENU mutations by high-throughput sequencing
Familial Feeling
Whole-exome sequencing identifies a novel germline variant in PTK7 gene in familial colorectal cancer
Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma [Letter]
Whole exome sequencing identifies APCDD1 and HDAC5 genes as potentially cancer predisposing in familial colorectal cancer
Familial chylomicronemia syndrome
Customized workflow development and data modularization concepts for RNA-Sequencing and metatranscriptome experiments
Monitoring rapid evolution of plant populations at scale with pool-sequencing
Genotyping of familial Mediterranean fever gene (MEFV)—Single nucleotide polymorphism—Comparison of Nanopore with conventional Sanger sequencing
Optimized and affordable high‐throughput sequencing workflow for preserved and nonpreserved small zooplankton specimens
Rapid Diagnosis of Familial Defective Apolipoprotein B-100
poreCov-An Easy to Use, Fast, and Robust Workflow for SARS-CoV-2 Genome Reconstruction via Nanopore Sequencing
Rapid identification of ENU mutations by high-throughput sequencing
Familial Feeling
Whole-exome sequencing identifies a novel germline variant in PTK7 gene in familial colorectal cancer
Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma [Letter]
Whole exome sequencing identifies APCDD1 and HDAC5 genes as potentially cancer predisposing in familial colorectal cancer
Familial chylomicronemia syndrome
Customized workflow development and data modularization concepts for RNA-Sequencing and metatranscriptome experiments
Monitoring rapid evolution of plant populations at scale with pool-sequencing
Genotyping of familial Mediterranean fever gene (MEFV)—Single nucleotide polymorphism—Comparison of Nanopore with conventional Sanger sequencing