Fredrik Dahl
Fredrik Dahl
Colibri Ventures
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Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
R Drmanac, AB Sparks, MJ Callow, AL Halpern, NL Burns, BG Kermani, ...
Science 327 (5961), 78-81, 2010
Multiplex amplification of large sets of human exons
GJ Porreca, K Zhang, JB Li, B Xie, D Austin, SL Vassallo, EM LeProust, ...
Nature methods 4 (11), 931-936, 2007
BLUEPRINT to decode the epigenetic signature written in blood
D Adams, L Altucci, SE Antonarakis, J Ballesteros, S Beck, A Bird, C Bock, ...
Nature biotechnology 30 (3), 224-226, 2012
Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells
BA Peters, BG Kermani, AB Sparks, O Alferov, P Hong, A Alexeev, Y Jiang, ...
Nature 487 (7406), 190-195, 2012
Multigene amplification and massively parallel sequencing for cancer mutation discovery
F Dahl, J Stenberg, S Fredriksson, K Welch, M Zhang, M Nilsson, ...
Proceedings of the National Academy of Sciences 104 (22), 9387-9392, 2007
Circle-to-circle amplification for precise and sensitive DNA analysis
F Dahl, J Banér, M Gullberg, M Mendel-Hartvig, U Landegren, M Nilsson
Proceedings of the National Academy of Sciences 101 (13), 4548-4553, 2004
Multiplex amplification enabled by selective circularization of large sets of genomic DNA fragments
F Dahl, M Gullberg, J Stenberg, U Landegren, M Nilsson
Nucleic acids research 33 (8), e71-e71, 2005
Real‐time monitoring of rolling‐circle amplification using a modified molecular beacon design
M Nilsson, M Gullberg, F Dahl, K Szuhai, AK Raap
Nucleic Acids Research 30 (14), e66-e66, 2002
Nucleic acid sequencing and process
R Drmanac, M Callow
US Patent 8,518,640, 2013
Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease
NT Ventham, NA Kennedy, AT Adams, R Kalla, S Heath, KR O'leary, ...
Nature communications 7 (1), 1-14, 2016
Analyzing genes using closing and replicating circles
M Nilsson, F Dahl, C Larsson, M Gullberg, J Stenberg
TRENDS in Biotechnology 24 (2), 83-88, 2006
Multiplex amplification of all coding sequences within 10 cancer genes by Gene-Collector
S Fredriksson, J Baner, F Dahl, A Chu, H Ji, K Welch, RW Davis
Nucleic acids research 35 (7), e47, 2007
Padlock and proximity probes for in situ and array‐based analyses: tools for the post‐genomic era
U Landegren, F Dahl, M Nilsson, S Fredriksson, J Banér, M Gullberg, ...
Comparative and functional genomics 4 (5), 525-530, 2003
Making ends meet in genetic analysis using padlock probes
M Nilsson, J Banér, M Mendel‐Hartvig, F Dahl, DO Antson, M Gullberg, ...
Human mutation 19 (4), 410-415, 2002
Molecular tools for a molecular medicine: analyzing genes, transcripts and proteins using padlock and proximity probes
U Landegren, E Schallmeiner, M Nilsson, S Fredriksson, J Banér, ...
Journal of Molecular Recognition 17 (3), 194-197, 2004
Methods and oligonucleotide designs for insertion of multiple adaptors into library constructs
F Dahl, R Drmanac, A Sparks
US Patent 7,897,344, 2011
Efficient base determination in sequencing reactions
R Drmanac, M Callow
US Patent 8,551,702, 2013
MLGA—a rapid and cost-efficient assay for gene copy-number analysis
M Isaksson, J Stenberg, F Dahl, AC Thuresson, ML Bondeson, M Nilsson
Nucleic acids research 35 (17), e115, 2007
PieceMaker: selection of DNA fragments for selector-guided multiplex amplification
J Stenberg, F Dahl, U Landegren, M Nilsson
Nucleic acids research 33 (8), e72-e72, 2005
Method for amplifying specific nucleic acids in parallel
F Dahl
US Patent 7,883,849, 2011
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Artículos 1–20