Using Illumina sequencing, one replicate of the virus library was sequenced in one run and three additional technical replicates were sequenced in a separate run. Thus, the four technical replicates were sequenced in two independent runs. The UpSet plot shows the number of barcodes that intersect amongst the four virus library technical replicates (lower panel), as well as the total counts of those barcodes in blue (upper panel). The libraries were clustered using L3 distance and a 99% reads cutoff was applied. The four replicates show a large degree of overlap in clustered barcodes.</p
Background: High throughput sequencing is frequently used to discover the location of regulatory int...
Raw Illumina sequence reads for 34 individuals, demultiplexed by individual barcode tags. Within ea...
<p>(<b>A</b>) Description of sequencing libraries. Except for J and K, each sample block (A through ...
A. L3 clustering distance of barcodes along with a 99% cumulative count cutoff was applied to the th...
<p>(A) Summary of the sample conditions. (B) Read distribution of three representative libraries. Fo...
For each barcode its log10 percentage of counts in the plasmid library is plotted on the x-axis, and...
The concept of a nucleic acid barcode applied to pathogen genomes is easy to grasp and the many poss...
The control spiked-in barcode is shown as purple bars, erroneous barcodes are shown as gray bars. Sh...
The y-axis depicts the barcode sequence; the x-axis shows the square root-transformed percentage of ...
<p>Three overlapping clones as revealed by barcoded sequencing (above) and pooled sequencing (below)...
<p>Once all the forward and reverse reads from the Illumina sequencer are joined one can see – in gr...
Applying a cutoff for barcode abundance eliminates most recall of longer barcodes that were not inte...
(A) Schematic representation of the sequences modified in #105B for the addition individual barcodes...
Linker sequences are trimmed with Cutadapt (colors represent distinct barcodes). Clustering is perfo...
<p>For each barcode, the x-axis is the list of all unique combinations of 4-mers arranged in the alp...
Background: High throughput sequencing is frequently used to discover the location of regulatory int...
Raw Illumina sequence reads for 34 individuals, demultiplexed by individual barcode tags. Within ea...
<p>(<b>A</b>) Description of sequencing libraries. Except for J and K, each sample block (A through ...
A. L3 clustering distance of barcodes along with a 99% cumulative count cutoff was applied to the th...
<p>(A) Summary of the sample conditions. (B) Read distribution of three representative libraries. Fo...
For each barcode its log10 percentage of counts in the plasmid library is plotted on the x-axis, and...
The concept of a nucleic acid barcode applied to pathogen genomes is easy to grasp and the many poss...
The control spiked-in barcode is shown as purple bars, erroneous barcodes are shown as gray bars. Sh...
The y-axis depicts the barcode sequence; the x-axis shows the square root-transformed percentage of ...
<p>Three overlapping clones as revealed by barcoded sequencing (above) and pooled sequencing (below)...
<p>Once all the forward and reverse reads from the Illumina sequencer are joined one can see – in gr...
Applying a cutoff for barcode abundance eliminates most recall of longer barcodes that were not inte...
(A) Schematic representation of the sequences modified in #105B for the addition individual barcodes...
Linker sequences are trimmed with Cutadapt (colors represent distinct barcodes). Clustering is perfo...
<p>For each barcode, the x-axis is the list of all unique combinations of 4-mers arranged in the alp...
Background: High throughput sequencing is frequently used to discover the location of regulatory int...
Raw Illumina sequence reads for 34 individuals, demultiplexed by individual barcode tags. Within ea...
<p>(<b>A</b>) Description of sequencing libraries. Except for J and K, each sample block (A through ...