<p>Number of analyzed RNA and DNA sequences in the study (after alignment to Galgal4).</p
<p>The number of samples for the identification of DNA methylation patterns and differentially methy...
Number of genes, samples, and class cardinality in each cancer-related microarray data set.</p
The list of detected genes with direct or inverted repeats of 17 or more nucleotides in length.</p
Number of RNA-Seq reads showing complete homology to viral reference sequences.</p
<p>List of samples examined in this study and the accession numbers of DNA sequences.</p
<p>Number of RNA-DNA sequence differences removed by various bioinformatics filters.</p
Number of transitions and transversion of nucleotide in genotyping by sequencing analysis.</p
<p>Number of nucleotide and indel characters and parsimony informative sites under the four alignmen...
<p>Number of sequenced reads (50 nucleotide long in average) and of nucleotides after SOLiD sequenci...
<p>Number of genes with expression detected in each category generated by the analysis of microarray...
<p>Summary of four SNPs (identified by sequence alignment) with their position, variation, frequency...
<p>Number of sequences obtained after sequence processing, after subtracting sequences detected also...
<p>Accession numbers of the specimens sequences, vouchers and DNA sequences analyzed.</p
<p>Number of GENSCAN gene models connected through RNA-seq alignments, with increasing requirements ...
<p>Coverage of alignment is the percent sequence coverage in 9,799,170 nucleotide long alignment.</p
<p>The number of samples for the identification of DNA methylation patterns and differentially methy...
Number of genes, samples, and class cardinality in each cancer-related microarray data set.</p
The list of detected genes with direct or inverted repeats of 17 or more nucleotides in length.</p
Number of RNA-Seq reads showing complete homology to viral reference sequences.</p
<p>List of samples examined in this study and the accession numbers of DNA sequences.</p
<p>Number of RNA-DNA sequence differences removed by various bioinformatics filters.</p
Number of transitions and transversion of nucleotide in genotyping by sequencing analysis.</p
<p>Number of nucleotide and indel characters and parsimony informative sites under the four alignmen...
<p>Number of sequenced reads (50 nucleotide long in average) and of nucleotides after SOLiD sequenci...
<p>Number of genes with expression detected in each category generated by the analysis of microarray...
<p>Summary of four SNPs (identified by sequence alignment) with their position, variation, frequency...
<p>Number of sequences obtained after sequence processing, after subtracting sequences detected also...
<p>Accession numbers of the specimens sequences, vouchers and DNA sequences analyzed.</p
<p>Number of GENSCAN gene models connected through RNA-seq alignments, with increasing requirements ...
<p>Coverage of alignment is the percent sequence coverage in 9,799,170 nucleotide long alignment.</p
<p>The number of samples for the identification of DNA methylation patterns and differentially methy...
Number of genes, samples, and class cardinality in each cancer-related microarray data set.</p
The list of detected genes with direct or inverted repeats of 17 or more nucleotides in length.</p
DOI
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