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Systematic assessment of commercially available low-input miRNA library preparation kits.
Heinicke F, Zhong X, Zucknick M, Breidenbach J, Sundaram AYM, T Flåm S, Leithaug M, Dalland M, Farmer A, Henderson JM, Hussong MA, Moll P, Nguyen L, McNulty A, Shaffer JM, Shore S, Yip HK, Vitkovska J, Rayner S, Lie BA, Gilfillan GD. Heinicke F, et al. Among authors: dalland m. RNA Biol. 2020 Jan;17(1):75-86. doi: 10.1080/15476286.2019.1667741. Epub 2019 Sep 27. RNA Biol. 2020. PMID: 31559901 Free PMC article.
Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing.
Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD. Bjørnstad PM, et al. Among authors: dalland m. Eur J Hum Genet. 2024 Jan 4. doi: 10.1038/s41431-023-01519-1. Online ahead of print. Eur J Hum Genet. 2024. PMID: 38172175 No abstract available.
A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing.
Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD. Bjørnstad PM, et al. Among authors: dalland m. Eur J Hum Genet. 2023 Nov 29. doi: 10.1038/s41431-023-01494-7. Online ahead of print. Eur J Hum Genet. 2023. PMID: 38030917