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Room 1
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Whole genome sequencing, variant calling
|
Malin Larsson, Nina Norgren
|
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Room 2
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Bulk RNA-Seq, small RNA-Seq
|
Julie Lorent, Johan Reimegård, Roy Francis
|
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Room 3
|
Single-cell RNA-Seq
|
Åsa Björklund, Paulo Czarnewski
|
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Room 4
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Genome and transcriptome assembly, annotation
|
Lucile Soler, Mahesh Panchal
|
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Room 5
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Epigenetics, Chip-Seq, Crispr-Cas
|
Agata Smialowska
|
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Room 6
|
Metagenomics
|
Dag Ahrén, Lokeshwaran Manoharan
|
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Room 7
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NGI, wet-lab, library-prep, long-read sequencing
|
Olga Petterson, Adam Ameur
|
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Room 8
|
Bash, Uppmax, Computing
|
Martin Dahlö
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