Search Results - "Schmid, Katharina T"

scPower accelerates and optimizes the design of multi-sample single cell transcriptomic studies by Schmid, Katharina T., Höllbacher, Barbara, Cruceanu, Cristiana, Böttcher, Anika, Lickert, Heiko, Binder, Elisabeth B., Theis, Fabian J., Heinig, Matthias

“…Single cell RNA-seq has revolutionized transcriptomics by providing cell type resolution for differential gene expression and expression quantitative trait…”
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epiAneufinder identifies copy number alterations from single-cell ATAC-seq data by Ramakrishnan, Akshaya, Symeonidi, Aikaterini, Hanel, Patrick, Schmid, Katharina T., Richter, Maria L., Schubert, Michael, Colomé-Tatché, Maria

“…Single-cell open chromatin profiling via scATAC-seq has become a mainstream measurement of open chromatin in single-cells. Here we present epiAneufinder, an…”
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Identification of genetic variants that impact gene co-expression relationships using large-scale single-cell data by Li, Shuang, Schmid, Katharina T, de Vries, Dylan H, Korshevniuk, Maryna, Losert, Corinna, Oelen, Roy, van Blokland, Irene V, Groot, Hilde E, Swertz, Morris A, van der Harst, Pim, Westra, Harm-Jan, van der Wijst, Monique G P, Heinig, Matthias, Franke, Lude

“…Expression quantitative trait loci (eQTL) studies show how genetic variants affect downstream gene expression. Single-cell data allows reconstruction of…”
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Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function by Hawe, Johann S, Wilson, Rory, Schmid, Katharina T, Zhou, Li, Lakshmanan, Lakshmi Narayanan, Lehne, Benjamin C, Kühnel, Brigitte, Scott, William R, Wielscher, Matthias, Yew, Yik Weng, Baumbach, Clemens, Lee, Dominic P, Marouli, Eirini, Bernard, Manon, Pfeiffer, Liliane, Matías-García, Pamela R, Autio, Matias I, Bourgeois, Stephane, Herder, Christian, Karhunen, Ville, Meitinger, Thomas, Prokisch, Holger, Rathmann, Wolfgang, Roden, Michael, Sebert, Sylvain, Shin, Jean, Strauch, Konstantin, Zhang, Weihua, Tan, Wilson L W, Hauck, Stefanie M, Merl-Pham, Juliane, Grallert, Harald, Barbosa, Eudes G V, Illig, Thomas, Peters, Annette, Paus, Tomas, Pausova, Zdenka, Deloukas, Panos, Foo, Roger S Y, Jarvelin, Marjo-Riitta, Kooner, Jaspal S, Loh, Marie, Heinig, Matthias, Gieger, Christian, Waldenberger, Melanie, Chambers, John C, Ahmadi, Kourosh R, Ainali, Chrysanthi, Barrett, Amy, Bataille, Veronique, Bell, Jordana T, Buil, Alfonso, Dermitzakis, Emmanouil T, Dimas, Antigone S, Durbin, Richard, Glass, Daniel, Grundberg, Elin, Hassanali, Neelam, Hedman, Åsa K, Ingle, Catherine, Knowles, David, Krestyaninova, Maria, Lindgren, Cecilia M, Lowe, Christopher E, McCarthy, Mark I, Meduri, Eshwar, di Meglio, Paola, Min, Josine L, Montgomery, Stephen B, Nestle, Frank O, Nica, Alexandra C, Nisbet, James, O'Rahilly, Stephen, Parts, Leopold, Potter, Simon, Sandling, Johanna, Sekowska, Magdalena, Shin, So-Youn, Small, Kerrin S, Soranzo, Nicole, Spector, Tim D, Surdulescu, Gabriela, Travers, Mary E, Tsaprouni, Loukia, Tsoka, Sophia, Wilk, Alicja, Yang, Tsun-Po, Zondervan, Krina T

“…We determined the relationships between DNA sequence variation and DNA methylation using blood samples from 3,799 Europeans and 3,195 South Asians. We identify…”
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