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Evaluation of commercially available RNA amplification kits for RNA sequencing using very low input amounts of total RNA.
Shanker S, Paulson A, Edenberg HJ, Peak A, Perera A, Alekseyev YO, Beckloff N, Bivens NJ, Donnelly R, Gillaspy AF, Grove D, Gu W, Jafari N, Kerley-Hamilton JS, Lyons RH, Tepper C, Nicolet CM. Shanker S, et al. Among authors: lyons rh. J Biomol Tech. 2015 Apr;26(1):4-18. doi: 10.7171/jbt.15-2601-001. J Biomol Tech. 2015. PMID: 25649271 Free PMC article.
Sequencing of the Dutch elm disease fungus genome using the Roche/454 GS-FLX Titanium System in a comparison of multiple genomics core facilities.
Forgetta V, Leveque G, Dias J, Grove D, Lyons R Jr, Genik S, Wright C, Singh S, Peterson N, Zianni M, Kieleczawa J, Steen R, Perera A, Bintzler D, Adams S, Hintz W, Jacobi V, Bernier L, Levesque R, Dewar K. Forgetta V, et al. J Biomol Tech. 2013 Apr;24(1):39-49. doi: 10.7171/jbt.12-2401-005. J Biomol Tech. 2013. PMID: 23542132 Free PMC article.
Estimation of DNA contamination and its sources in genotyped samples.
Zajac GJM, Fritsche LG, Weinstock JS, Dagenais SL, Lyons RH, Brummett CM, Abecasis GR. Zajac GJM, et al. Among authors: lyons rh. Genet Epidemiol. 2019 Dec;43(8):980-995. doi: 10.1002/gepi.22257. Epub 2019 Aug 26. Genet Epidemiol. 2019. PMID: 31452258 Free PMC article.
Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs.
Pistis G, Porcu E, Vrieze SI, Sidore C, Steri M, Danjou F, Busonero F, Mulas A, Zoledziewska M, Maschio A, Brennan C, Lai S, Miller MB, Marcelli M, Urru MF, Pitzalis M, Lyons RH, Kang HM, Jones CM, Angius A, Iacono WG, Schlessinger D, McGue M, Cucca F, Abecasis GR, Sanna S. Pistis G, et al. Among authors: lyons rh. Eur J Hum Genet. 2015 Jul;23(7):975-83. doi: 10.1038/ejhg.2014.216. Epub 2014 Oct 8. Eur J Hum Genet. 2015. PMID: 25293720 Free PMC article.
High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation sequencing.
Halbritter J, Diaz K, Chaki M, Porath JD, Tarrier B, Fu C, Innis JL, Allen SJ, Lyons RH, Stefanidis CJ, Omran H, Soliman NA, Otto EA. Halbritter J, et al. Among authors: lyons rh. J Med Genet. 2012 Dec;49(12):756-67. doi: 10.1136/jmedgenet-2012-100973. J Med Genet. 2012. PMID: 23188109
Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria.
Ovunc B, Otto EA, Vega-Warner V, Saisawat P, Ashraf S, Ramaswami G, Fathy HM, Schoeb D, Chernin G, Lyons RH, Yilmaz E, Hildebrandt F. Ovunc B, et al. Among authors: lyons rh. J Am Soc Nephrol. 2011 Oct;22(10):1815-20. doi: 10.1681/ASN.2011040337. Epub 2011 Sep 8. J Am Soc Nephrol. 2011. PMID: 21903995 Free PMC article.
88 results