Publikationen von M. Lienhard
Alle Typen
Zeitschriftenartikel (34)
21.
Zeitschriftenartikel
48 (6), S. 593 - 599 (2016)
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences. Nature Genetics 22.
Zeitschriftenartikel
526 (7571), S. 68 - 74 (2015)
A global reference for human genetic variation. Nature 23.
Zeitschriftenartikel
112 (31), S. E4236 - E4245 (2015)
Simultaneous deletion of the methylcytosine oxidases Tet1 and Tet3 increases transcriptome variability in early embryogenesis. Proceedings of the National Academy of Sciences of the United States of America 24.
Zeitschriftenartikel
17 (5), S. 545 - 557 (2015)
The histone deacetylase SIRT6 controls embryonic stem cell fate via TET-mediated production of 5-hydroxymethylcytosine. Nature Cell Biology 25.
Zeitschriftenartikel
42 (14), e110 (2014)
ARH-seq: identification of differential splicing in RNA-seq data. Nucleic Acids Research (London) 26.
Zeitschriftenartikel
15 (8), S. 777 - 788 (2014)
Epigenomic analysis of primary human T cells reveals enhancers associated with TH2 memory cell differentiation and asthma susceptibility. Nature Immunology 27.
Zeitschriftenartikel
5, 5:3934 (2014)
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel. Nature Communications 28.
Zeitschriftenartikel
30 (2), S. 284 - 286 (2014)
MEDIPS: genome-wide differential coverage analysis of sequencing data derived from DNA enrichment experiments. Bioinformatics 29.
Zeitschriftenartikel
30 (2), S. 284 - 286 (2014)
MEDIPS: genome wide differential coverage analysis of sequencing data derived from DNA enrichment experiments. Bioinformatics 30.
Zeitschriftenartikel
30 (2), S. 284 - 286 (2014)
MEDIPS: genome-wide differential coverage analysis of sequencing data derived from DNA enrichment experiments. Bioinformatics 31.
Zeitschriftenartikel
342 (6154), S. 1235587 - 1235587 (2013)
Integrative annotation of variants from 1092 humans: application to cancer genomics. Science 32.
Zeitschriftenartikel
9 (2), S. e1003250 - e1003250 (2013)
DNA–Methylome Analysis of Mouse Intestinal Adenoma Identifies a Tumour-Specific Signature That Is Partly Conserved in Human Colon Cancer. PLoS Genetics 33.
Zeitschriftenartikel
130 (2), S. 427 - 439 (2012)
RNA-Seq provides new insights in the transcriptome responses induced by the carcinogen benzo[a]pyrene. Toxicological Sciences 34.
Zeitschriftenartikel
491 (7422), S. 56 - 65 (2012)
An integrated map of genetic variation from 1,092 human genomes. Nature Buchkapitel (1)
35.
Buchkapitel
Quantitative Comparison of Large-Scale DNA Enrichment Sequencing Data. In: Statistical Genomics (Hg. Mathé, E.; Davis, S.) (2016)
Hochschulschrift - Doktorarbeit (1)
36.
Hochschulschrift - Doktorarbeit
Computational Analysis of Genome-wide Methylation Enrichment Experiments. Dissertation, xii, 125 S. (2017)
Hochschulschrift - Master (1)
37.
Hochschulschrift - Master
Analysis of RNA-seq experiments. Master, Freie Universität, Berlin (2011)
Preprint (2)
38.
Preprint
Systematic assessment of long-read RNA-seq methods for transcript identification and quantification. (2023)
39.
Preprint
Long-read transcriptome sequencing analysis with IsoTools. (2021)