Márton Münz

发表

BCR repertoire sequencing: different patterns of B cell activation after two Meningococcal vaccines

Johannes Trück, Anna Fowler, Gerton Lunter, 2015, Immunology and cell biology.

In-Depth Assessment of Within-Individual and Inter-Individual Variation in the B Cell Receptor Repertoire

Johannes Trück, Anna Fowler, Gerton Lunter, 2015, Front. Immunol..

The Role of Flexibility and Conformational Selection in the Binding Promiscuity of PDZ Domains

Jotun Hein, Philip C. Biggin, Márton Münz, 2012, PLoS Comput. Biol..

CoverView: a sequence quality evaluation tool for next generation sequencing data

S. Seal, N. Rahman, S. Mahamdallie, 2018, Wellcome open research.

Dynamics based alignment of proteins: an alternative approach to quantify dynamic similarity

Jotun Hein, Philip C. Biggin, Márton Münz, 2010, BMC Bioinformatics.

CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting

Nazneen Rahman, Gerton Lunter, Shazia Mahamdallie, 2015, Genome Medicine.

JGromacs: A Java Package for Analyzing Protein Simulations

Philip C. Biggin, Márton Münz, P. Biggin, 2011, J. Chem. Inf. Model..

Analysis of B Cell Repertoire Dynamics Following Hepatitis B Vaccination in Humans, and Enrichment of Vaccine-specific Antibody Sequences

Johannes Trück, Anna Fowler, Gerton Lunter, 2015, EBioMedicine.

ICR142 Benchmarker: evaluating, optimising and benchmarking variant calling performance using the ICR142 NGS validation series

Nazneen Rahman, Shazia Mahamdallie, Elise Ruark, 2018, Wellcome open research.

ICR142 Benchmarker: evaluating, optimising and benchmarking variant calling performance using the ICR142 NGS validation series

N. Rahman, S. Ellard, A. Renwick, 2018, Wellcome Open Research.

OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis

Nazneen Rahman, Gerton Lunter, Elise Ruark, 2016, Scientific Reports.

Clinical Annotation Reference Templates: a resource for consistent variant annotation

Nazneen Rahman, Shazia Mahamdallie, Elise Ruark, 2018, Wellcome Open Research.

CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting

S. Seal, N. Rahman, G. Lunter, 2015, Genome Medicine.

The ICR1000 UK exome series: a resource of gene variation in an outbred population

S. Seal, N. Rahman, A. Renwick, 2015, F1000Research.

The Quality Sequencing Minimum (QSM): providing comprehensive, consistent, transparent next generation sequencing data quality assurance

Shazia Mahamdallie, Elise Ruark, Shawn Yost, 2018, Wellcome open research.

The Quality Sequencing Minimum (QSM): providing comprehensive, consistent, transparent next generation sequencing data quality assurance [version 1; peer review: 2 approved, 1 approved with reservations]

S. Seal, N. Rahman, A. Renwick, 2021 .

ICR142 Benchmarker: evaluating, optimising and benchmarking variant calling performance using the ICR142 NGS validation series

N. Rahman, S. Ellard, A. Renwick, 2018, Wellcome open research.

ICR142 Benchmarker: evaluating, optimising and benchmarking variant calling using the ICR142 NGS validation series [version 1; peer review: 2 approved with reservations]

N. Rahman, S. Ellard, A. Renwick, 2021 .

Previously titled: ICR142 Benchmarker: evaluating, optimising and benchmarking variant calling using the ICR142 NGS validation series

A. Renwick, Esty Holt, S. Mahamdallie, 2018 .