檢索結果 - Lappalainen, Tuuli

From trainee to tenure-track: ten tips 由 Lappalainen, Tuuli

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Functional genomics bridges the gap between quantitative genetics and molecular biology 由 Lappalainen, Tuuli

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A polyclonal allelic expression assay for detecting regulatory effects of transcript variants 由 Brandt, Margot, Gokden, Alper, Ziosi, Marcello, Lappalainen, Tuuli

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Rare and Common Regulatory Variation in Population-Scale Sequenced Human Genomes 由 Montgomery, Stephen B., Lappalainen, Tuuli, Gutierrez-Arcelus, Maria, Dermitzakis, Emmanouil T.

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Epistatic Selection between Coding and Regulatory Variation in Human Evolution and Disease 由 Lappalainen, Tuuli, Montgomery, Stephen B., Nica, Alexandra C., Dermitzakis, Emmanouil T.

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Allelic mapping bias in RNA-sequencing is not a major confounder in eQTL studies 由 Panousis, Nikolaos I, Gutierrez-Arcelus, Maria, Dermitzakis, Emmanouil T, Lappalainen, Tuuli

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Quantifying the regulatory effect size of cis-acting genetic variation using allelic fold change 由 Mohammadi, Pejman, Castel, Stephane E., Brown, Andrew A., Lappalainen, Tuuli

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Genomic analysis in the age of human genome sequencing 由 Lappalainen, Tuuli, Scott, Alexandra J, Brandt, Margot, Hall, Ira M

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Tools and best practices for data processing in allelic expression analysis 由 Castel, Stephane E., Levy-Moonshine, Ami, Mohammadi, Pejman, Banks, Eric, Lappalainen, Tuuli

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Rare variant phasing and haplotypic expression from RNA sequencing with phASER 由 Castel, Stephane E., Mohammadi, Pejman, Chung, Wendy K., Shen, Yufeng, Lappalainen, Tuuli

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A vast resource of allelic expression data spanning human tissues 由 Castel, Stephane E., Aguet, François, Mohammadi, Pejman, Ardlie, Kristin G., Lappalainen, Tuuli

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Tandem RNA Chimeras Contribute to Transcriptome Diversity in Human Population and Are Associated with Intronic Genetic Variants 由 Greger, Liliana, Su, Jing, Rung, Johan, Ferreira, Pedro G., Lappalainen, Tuuli, Dermitzakis, Emmanouil T., Brazma, Alvis

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MBV: a method to solve sample mislabeling and detect technical bias in large combined genotype and sequencing assay datasets 由 Fort, Alexandre, Panousis, Nikolaos I, Garieri, Marco, Antonarakis, Stylianos E, Lappalainen, Tuuli, Dermitzakis, Emmanouil T, Delaneau, Olivier

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Integrative approach identifies SLC6A20 and CXCR6 as putative causal genes for the COVID-19 GWAS signal in the 3p21.31 locus 由 Kasela, Silva, Daniloski, Zharko, Jordan, Tristan X., tenOever, Benjamin R., Sanjana, Neville E., Lappalainen, Tuuli

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Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs 由 Hannelius, Ulf, Salmela, Elina, Lappalainen, Tuuli, Guillot, Gilles, Lindgren, Cecilia M, von Döbeln, Ulrika, Lahermo, Päivi, Kere, Juha

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Assessing allele-specific expression across multiple tissues from RNA-seq read data 由 Pirinen, Matti, Lappalainen, Tuuli, Zaitlen, Noah A., Dermitzakis, Emmanouil T., Donnelly, Peter, McCarthy, Mark I., Rivas, Manuel A.

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Leveraging allelic imbalance to refine fine-mapping for eQTL studies 由 Zou, Jennifer, Hormozdiari, Farhad, Jew, Brandon, Castel, Stephane E., Lappalainen, Tuuli, Ernst, Jason, Sul, Jae Hoon, Eskin, Eleazar

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Integrative approach identifies SLC6A20 and CXCR6 as putative causal genes for the COVID-19 GWAS signal in the 3p21.31 locus 由 Kasela, Silva, Daniloski, Zharko, Bollepalli, Sailalitha, Jordan, Tristan X., tenOever, Benjamin R., Sanjana, Neville E., Lappalainen, Tuuli

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Genomic landscape of positive natural selection in Northern European populations 由 Lappalainen, Tuuli, Salmela, Elina, Andersen, Peter M, Dahlman-Wright, Karin, Sistonen, Pertti, Savontaus, Marja-Liisa, Schreiber, Stefan, Lahermo, Päivi, Kere, Juha

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Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk 由 Castel, Stephane E., Cervera, Alejandra, Mohammadi, Pejman, Aguet, François, Reverter, Ferran, Wolman, Aaron, Guigo, Roderic, Iossifov, Ivan, Vasileva, Ana, Lappalainen, Tuuli

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