<p>After filtering the only adaptor sequences, containing N sequences and low quality sequences, the RNA-Seq libraries of SKPs and SFBs generated over 19 million clean reads each, and the percentage of clean reads among raw tags in each library ranged from 95.95% to 98.38%.</p
<p>Libraries were retrieved by next generation semiconductor sequencing technology. Number of reads ...
We have successfully constructed 30 saker cDNA libraries, and RNA-seq produced a total of 107.56 Gb ...
(A) The proportion of reads from single-species libraries that were incorrectly mapped to the wrong ...
<p>The number and percentage (in parentheses) of the sequences removed for redundant (column 2) and ...
<p>Reads were aligned to reference sequences by allowing two mismatches.</p><p>Read counts and perce...
<p>Clean reads are those remaining after low-quality reads have been removed from total raw reads. U...
<p>3ADT&length filter: reads removed due to 3ADT not found and length with <17 nt and>25 nt were rem...
<p>The percentages of tags containing N, adaptors, clean tags and low quality reads. The numbers in ...
n of raw strand specific lot of raw reads. Thus, RNASeqBrowser collapses exact duplicate reads to re...
<p>To obtain mappable sequences from raw sequencing data, we used a series of digital filters to rem...
<p>The number of raw sequence read pairs generated as well as the number of collapsed trimmed reads ...
<p>All DNA:RNA mismatches have a minimum read depth of 3X and at least 5% of total reads and 3 indiv...
<p>Total read number generated by Illumina RNA-seq and following quality control measures including ...
<p>Indicated from left to right are the numbers of reads that passed quality filtering (clean reads)...
<p>Raw Reads - the total number of reads generated by each sequencing run; Full Length Reads - the t...
<p>Libraries were retrieved by next generation semiconductor sequencing technology. Number of reads ...
We have successfully constructed 30 saker cDNA libraries, and RNA-seq produced a total of 107.56 Gb ...
(A) The proportion of reads from single-species libraries that were incorrectly mapped to the wrong ...
<p>The number and percentage (in parentheses) of the sequences removed for redundant (column 2) and ...
<p>Reads were aligned to reference sequences by allowing two mismatches.</p><p>Read counts and perce...
<p>Clean reads are those remaining after low-quality reads have been removed from total raw reads. U...
<p>3ADT&length filter: reads removed due to 3ADT not found and length with <17 nt and>25 nt were rem...
<p>The percentages of tags containing N, adaptors, clean tags and low quality reads. The numbers in ...
n of raw strand specific lot of raw reads. Thus, RNASeqBrowser collapses exact duplicate reads to re...
<p>To obtain mappable sequences from raw sequencing data, we used a series of digital filters to rem...
<p>The number of raw sequence read pairs generated as well as the number of collapsed trimmed reads ...
<p>All DNA:RNA mismatches have a minimum read depth of 3X and at least 5% of total reads and 3 indiv...
<p>Total read number generated by Illumina RNA-seq and following quality control measures including ...
<p>Indicated from left to right are the numbers of reads that passed quality filtering (clean reads)...
<p>Raw Reads - the total number of reads generated by each sequencing run; Full Length Reads - the t...
<p>Libraries were retrieved by next generation semiconductor sequencing technology. Number of reads ...
We have successfully constructed 30 saker cDNA libraries, and RNA-seq produced a total of 107.56 Gb ...
(A) The proportion of reads from single-species libraries that were incorrectly mapped to the wrong ...
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