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To confirm this phenomenon, samples were mapped (Fig. 6), and areas in which Cl was found also contained Na.
The high-quality reads of all the samples were mapped to the published CBS 513.88 (Genbank Accession Number: GCA_000002855.2) genome.
The reads for each of the 46 samples were mapped to the revised Cambridge reference mitochondrial sequence (NC012920.1) using the iterative mapping assembler MIA [13].
The reads from lanes 5, 6 and 8 corresponding to human cancer cell line samples were mapped to the human reference genome (hg19) by ELAND (Illumina).
The normalized copy number data obtained from the 227 samples were mapped into the human genome using the Build 18 (NCBI 36) assembly with an annotation file provided by the manufacturer (http://www.chem.agilent.com/).agilent.com/
Geographical locations of samples were mapped (Arcview 3.2, ESRI) and compared among the subgroups.
Forty-seven samples were mapped against a reference sequence to investigate heteroplasmy in mtDNA.
The collecting provinces and districts of all virus samples were mapped on the trees.
All together 570,094,697 high quality reads of 285 samples were mapped to Nipponbare reference.
Reads from four samples were mapped to the six assemblies separately.
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In cases that one gene symbol matches multiple probe set IDs, the probe set which shows the most variance across the samples was mapped to the gene.
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