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Zeitschriftenartikel (117)
101.
Zeitschriftenartikel
25 (12), S. 1840 - 8 (2011)
The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories. Leukemia: Official Journal of the Leukemia Society of America, Leukemia Research Fund, U.K 102.
Zeitschriftenartikel
29 (9), S. 1338 - 48 (2011)
Human induced pluripotent stem cells harbor homoplasmic and heteroplasmic mitochondrial DNA mutations while maintaining human embryonic stem cell-like metabolic reprogramming. Stem Cells 103.
Zeitschriftenartikel
30 (2), S. 199 - 210 (2011)
The power of NGS technologies to delineate the genome organization in cancer: from mutations to structural variations and epigenetic alterations. Cancer Metastasis Reviews 104.
Zeitschriftenartikel
5 (12), S. e15661 - e15661 (2010)
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis. PLoS ONE 105.
Zeitschriftenartikel
31 (suppl 2), S. 255 - 257 (2010)
High-throughput sequencing of frozen and paraffin-embedded tumor and normal tissue. Pathologe 106.
Zeitschriftenartikel
20, S. 1441 - 1450 (2010)
Computational analysis of genome-wide DNA methylation during the differentiation of human embryonic stem cells along the endodermal lineage. Genome Research 107.
Zeitschriftenartikel
2 (8), S. 475 - 486 (2010)
A new dominant peroxiredoxin allele identified by whole-genome re-sequencing of random mutagenized yeast causes oxidant-resistance and premature aging. Aging (Albany NY) 108.
Zeitschriftenartikel
2, S. 2:59 - 2:59 (2010)
The application of massively parallel sequencing technologies in diagnostics. F1000 Biology Reports 109.
Zeitschriftenartikel
High-throughput sequencing of microdissected chromosomal regions. European Journal of Human Genetics, ejhg.2009.196, S. 1 - 6 (2009)
110.
Zeitschriftenartikel
4 (5), S. e5548 - e5548 (2009)
Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysis. PLoS ONE 111.
Zeitschriftenartikel
9, S. 9:38 - 9:38 (2008)
Sequencing and genotypic analysis of the triosephosphate isomerase (TPI1) locus in a large sample of long-lived Germans. BMC Genetics 112.
Zeitschriftenartikel
9, S. 9:38 - 9:38 (2008)
Sequencing and genotypic analysis of the triosephosphate isomerase (TPI1) locus in a large sample of long-lived Germans. BMC Genetics 113.
Zeitschriftenartikel
5 (5), S. 31 - 32 (2004)
Genetische Variabilität des Menschen: Hochdurchsatz- Technologien und Datenanalyse. Laborwelt 114.
Zeitschriftenartikel
2004 (1), S. 17 - 19 (2004)
Vergleichende Sequenzierung von Kandidatengenen: die Resequencing-Plattform am MPI-MG. GenomXPress: Informationen aus der Deutschen Genomforschung 115.
Zeitschriftenartikel
4 (6), S. 351 - 378 (2003)
Human inter-individual DNA sequence variation in candidate genes, drug targets, the importance of haplotypes and pharmacogenomics. Current Pharmaceutical Biotechnology 116.
Zeitschriftenartikel
61 (1 - 2), S. 97 - 109 (2002)
Beta-2 Adrenergic receptor gene variations and coping styles in twins. Biological Psychology 117.
Zeitschriftenartikel
Haplotypen und die systematische Analyse genetischer Variation: Krankheitsgene, „Drug Targets“ und Pharmakogenomik. Proteomics & Drug Development, S. 478 - 485 (2002)
Sonstige (3)
118.
Sonstige
The Developmental Transcriptome for Lytechinus variegatus Exhibits Temporally Punctuated Gene Expression Changes, bioRxiv (Preprint Server) 2019, (2020)
119.
Sonstige
Functional dissection of TADs reveals non-essential and instructive roles in regulating gene expression, bioRxiv (Preprint Server) 2019, (2019)
120.
Sonstige
Crowdfunded whole-genome sequencing of the celebrity cat Lil BUB identifies causal mutations for her osteopetrosis and polydactyly, bioRxiv (Preprint Server), (2019)