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Additionally, the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways annotation of unigenes was performed by mapping the sequences obtained from Blast2GO to the contents of KEGG database (Kanehisa and Goto 2000).
Also, we compared the SCS and bareback-processed samples after mapping the sequences to the genome.
The probe sequence accuracy was validated by mapping the sequences to the Ae. tauschii Illumina reads representing 30X genome coverage.
Further filtering was done by mapping the sequences containing SNPs to the E. guineensis genome scaffolds [ 1].
However, many inserts would not be detected by mapping the sequences to the reference genome, because they do not include sufficient mappable sequence.
After the completion of the human genome the location and structure of the human Sp8 gene was identified by mapping the sequences of Sp8L and Sp8S cDNA clones.
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We did this by mapping the sequence of the probes, and determining their position in the gene with regard to the miRNA target sites predicted for the gene.
High throughput re-sequencing uncovers various genetic variations by mapping the sequencing reads of related individuals to the reference genome.
By mapping the sequence reads back to pre-miRNAs, one can quantify the expression levels of mature miRNAs.
We mapped the sequences of hairpins instead of miRNAs to the mouse genome (mm7) using Blastn program.
We previously mapped the sequences of four transcriptional units from the A and B subfamilies onto their genomic blocks [ 15].
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