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Publications by Andreas Halman
Accuracy of Short Tandem Repeats Genotyping Tools in Whole Exome Sequencing Data
F1000Research
Genetics
Molecular Biology
Pharmacology
Biochemistry
Microbiology
Immunology
Medicine
Toxicology
Pharmaceutics
Related publications
Detecting Expansions of Tandem Repeats in Cohorts Sequenced With Short-Read Sequencing Data
American Journal of Human Genetics
Genetics
An Evaluation of Copy Number Variation Detection Tools for Cancer Using Whole Exome Sequencing Data
BMC Bioinformatics
Biochemistry
Applied Mathematics
Computer Science Applications
Structural Biology
Molecular Biology
Whole Exome Sequencing in Monogenic Dyslipidemias
Journal of Atherosclerosis and Thrombosis
Biochemistry
Internal Medicine
Cardiovascular Medicine
Cardiology
Digital Fragment Analysis of Short Tandem Repeats by High-Throughput Amplicon Sequencing
Ecology and Evolution
Evolution
Ecology
Nature
Systematics
Behavior
Landscape Conservation
Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
OC48 Re-Interrogation of Whole Exome Sequencing Data in Developmental Epileptic Encephalopathies
Clinical Application of Whole-Exome Sequencing
JAMA Neurology
Neurology
Targeted Genotyping of Variable Number Tandem Repeats With adVNTR
Genome Research
Genetics
Prediction and Prioritization of Neoantigens: Integration of RNA Sequencing Data With Whole-Exome Sequencing
Cancer Science
Cancer Research
Medicine
Oncology