Rezultati pretrage - Feuk, Lars

ASHG 2008 Annual Meeting: from enormous cohorts to individual genomes od Feuk, Lars

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Inversion variants in the human genome: role in disease and genome architecture od Feuk, Lars

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Exome RNA sequencing reveals rare and novel alternative transcripts od Halvardson, Jonatan, Zaghlool, Ammar, Feuk, Lars

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Global and unbiased detection of splice junctions from RNA-seq data od Ameur, Adam, Wetterbom, Anna, Feuk, Lars, Gyllensten, Ulf

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Transcriptome analysis of fibroblasts from schizophrenia patients reveals differential expression of schizophrenia-related genes od Etemadikhah, Mitra, Niazi, Adnan, Wetterberg, Lennart, Feuk, Lars

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Identification of novel exons and transcribed regions by chimpanzee transcriptome sequencing od Wetterbom, Anna, Ameur, Adam, Feuk, Lars, Gyllensten, Ulf, Cavelier, Lucia

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Strategies for the detection of copy number and other structural variants in the human genome od Carson, Andrew R, Feuk, Lars, Mohammed, Mansoor, Scherer, Stephen W

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Evaluation of Single-Molecule Sequencing Technologies for Structural Variant Detection in Two Swedish Human Genomes od Fatima, Nazeefa, Petri, Anna, Gyllensten, Ulf, Feuk, Lars, Ameur, Adam

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Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier od Eisfeldt, Jesper, Pettersson, Maria, Petri, Anna, Nilsson, Daniel, Feuk, Lars, Lindstrand, Anna

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Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants od Klar, Joakim, Engstrand-Lilja, Helene, Maqbool, Khurram, Mattisson, Jonas, Feuk, Lars, Dahl, Niklas

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Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissues od Zaghlool, Ammar, Ameur, Adam, Nyberg, Linnea, Halvardson, Jonatan, Grabherr, Manfred, Cavelier, Lucia, Feuk, Lars

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Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family od Lindholm Carlström, Eva, Halvardson, Jonatan, Etemadikhah, Mitra, Wetterberg, Lennart, Gustavson, Karl-Henrik, Feuk, Lars

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Characterization of the nuclear and cytosolic transcriptomes in human brain tissue reveals new insights into the subcellular distribution of RNA transcripts od Zaghlool, Ammar, Niazi, Adnan, Björklund, Åsa K., Westholm, Jakub Orzechowski, Ameur, Adam, Feuk, Lars

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Interpretable Machine Learning Reveals Dissimilarities Between Subtypes of Autism Spectrum Disorder od Garbulowski, Mateusz, Smolinska, Karolina, Diamanti, Klev, Pan, Gang, Maqbool, Khurram, Feuk, Lars, Komorowski, Jan

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The Database of Genomic Variants: a curated collection of structural variation in the human genome od MacDonald, Jeffrey R., Ziman, Robert, Yuen, Ryan K. C., Feuk, Lars, Scherer, Stephen W.

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Copy number of pancreatic polypeptide receptor gene NPY4R correlates with body mass index and waist circumference od Shebanits, Kateryna, Andersson-Assarsson, Johanna C., Larsson, Ingrid, Carlsson, Lena M. S., Feuk, Lars, Larhammar, Dan

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Copy number determination of the gene for the human pancreatic polypeptide receptor NPY4R using read depth analysis and droplet digital PCR od Shebanits, Kateryna, Günther, Torsten, Johansson, Anna C. V., Maqbool, Khurram, Feuk, Lars, Jakobsson, Mattias, Larhammar, Dan

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Robust and Accurate Single Nucleotide Polymorphism Genotyping by Dynamic Allele-Specific Hybridization (DASH): Design Criteria and Assay Validation od Prince, Jonathan A., Feuk, Lars, Howell, W. Mathias, Jobs, Magnus, Emahazion, Tesfai, Blennow, Kaj, Brookes, Anthony J.

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Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder od Hooper, Sean D, Johansson, Anna CV, Tellgren-Roth, Christian, Stattin, Eva-Lena, Dahl, Niklas, Cavelier, Lucia, Feuk, Lars

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Analyzing DNA methylation patterns in subjects diagnosed with schizophrenia using machine learning methods od Moghadam, Behrooz Torabi, Etemadikhah, Mitra, Rajkowska, Grazyna, Stockmeier, Craig, Grabherr, Manfred, Komorowski, Jan, Feuk, Lars, Carlström, Eva Lindholm

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