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Other basic parameters like number of reads per contig as well as the average coverage were comparable, constituting a suitable basis for alignment analyses of contigs.
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H3-similar hits were virtually translated into proteins and used for alignment analyses.
Consensus contigs developed across all 27 genotypes served as the basis for alignment to detect SNP.
Amino acid alignments were used to guide nucleotide alignments, which formed the basis for phylogenetic analyses.
An alignment that covers approximately 10,050 bp of Xist was then modified by removal of gaps and regions showing alignment ambiguity and was used as the basis for phylogenetic analyses.
At last, the new alignment has 1112 sequences, and this alignment becomes the basis for the following analyses.
Because use of the IUPAC nomenclature for biallelic SNPs yielded a closer to normal distribution of error than the other methods and was readily implemented in a single alignment strategy, we employed this technique on a transcriptome-wide basis for subsequent analyses.
Hence, it represents a suitable basis for automated analyses.
Therefore, this model provides a theoretical basis for further analyses.
These 8 countries served as the basis for our analyses.
NHANES 1999 2004 data form the basis for these analyses.
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