Sentence examples for dna was mapped from inspiring English sources

In 2008, much of the woolly mammoth's chromosomal DNA was mapped.

Labelled DNA was mapped to pachytene or late zygotene spreads which provide the best resolution for physical mapping by fluorescence in situ hybridisation.

These include the genera Megasphaera spp., Bacteroides spp., Coprococcus spp., and Clostridiales spp. Less than 1%% of DNA was mapped to lytic bacteriophages, members of genera I3likevirus, T4likevirus and Phikzlikevirus of the family Myoviridae.

Sequence data from genomic DNA was mapped to the reference human genome (hg19) using the Burrows-Wheeler Aligner™ and were processed using the publicly available Sequence Alignment/Map (SAMtools), Picard and Genome Analysis Toolkit (9, 10).

Once the DNA is mapped, the mammoth could find its place among its extinct and extant relatives.

Using computational methods, sequence patterns with potential to form G4 DNA were mapped within 32996 hotspots and corresponding flanking regions in human.

The reads of bisulfite converted DNA were mapped to Apis mellifera genome assembly 4 after converting the Cs to Ts.

A total of 14,216 DNaseI-hypersensitive (HS) sites, covering ~4.2 megabases of DNA, are mapped to the hg17 version (NCBI build 35) of the human genome sequence.

As indicated in Table 1, 837 Mb of the initial reads of control white blood cell DNA were mapped using the BWA program [ 19] to 58.9 Mb regions on the reference human genome (GRCh37.p2), including high quality mapping of 717 Mb reads to 10.6 Mb regions with minimum 10 times and average 67 times coverage.

In the first round, all progeny DNAs were mapped over the entire chromosome at 15-Mb resolution.

Sequenced DNAs were mapped into a Chicken Genome database (NCBI, Build 3.1) with a Burrows-Wheeler Aligner (BWA) version 0.6.1 program (Li and Durbin, 2009).