Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Emilia Mollova"'
Autor:
Greg Young, Aaron Wenger, Matthew Boitano, Armin Toepfer, Christine Lambert, Primo Baybayan, Emilia Mollova
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100639- (2023)
Externí odkaz:
https://doaj.org/article/c884c5b29cf64268bb028ce491f4b309
Autor:
David Hsu, James H. Bullard, Dale R. Webster, Jackie Yen, Ellen E. Paxinos, Lori A. Rowe, Susana Wang, Paul Peluso, John J. Mekalanos, Brigid M. Davis, Khai Luong, Jon M. Sorenson, Andrew Kasarskis, Marie Valdovino, Matthew K. Waldor, Amruta Joshi, Maryann Turnsek, Eric E. Schadt, Cheryl L. Tarr, Brianna Lamay, Michael Frace, Chen-Shan Chin, Robert Sebra, Emilia Mollova, Ali Bashir, William P. Robins, Aaron Klammer, Steven Lin, Meredith Ashby
Publikováno v:
Nature Biotechnology. 30:701-707
The multikilobase reads that can be produced by single-molecule sequencing technologies may span complex, repetitive genomic regions but have high error rates. Bashir et al. use these reads to organize contigs assembled from accurate, short-read data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a15d8723ca843cdd0b8a8d2eaa794df1
https://doi.org/10.1038/nbt.2288
https://doi.org/10.1038/nbt.2288
Autor:
Eric J. White, Sergey V. Fridrikh, Ekaterina Protozanova, Dirk Peter Ten Broeck, Douglas B. Cameron, Rudolf Gilmanshin, Emilia Mollova, Meng Zhang
Publikováno v:
Analytical Biochemistry. 402:83-90
Here we describe bacterial genotyping by direct linear analysis (DLA) single-molecule mapping. DLA involves preparation of restriction digest of genomic DNA labeled with a sequence-specific fluorescent probe and stained nonspecifically with intercala
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41402c6687ce1bbf16dd4cfdc19933eb
https://doi.org/10.1016/j.ab.2010.03.024
https://doi.org/10.1016/j.ab.2010.03.024
Publikováno v:
Analytical Biochemistry. 391:135-143
Existing methods for extraction and processing of large fragments of bacterial genomic DNA are manual, time-consuming, and prone to variability in DNA quality and recovery. To solve these problems, we have designed and built an automated fluidic syst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b3b0f2691b2b56129db7c7069f865c8
https://doi.org/10.1016/j.ab.2009.05.008
https://doi.org/10.1016/j.ab.2009.05.008