Publication date
December 2016
DOIAbstract
The number of reads from all samples after DNA sequnecing, obtained from the program R, and presented in excel
The number of reads from all samples after DNA sequnecing, obtained from the program R, and presented in excel
<p>Number of samples and percentage of samples identified using DNA barcoding, photo identification ...
<p>Number of analyzed RNA and DNA sequences in the study (after alignment to Galgal4).</p
<p>Number of reads after each step of processing and taxonomy mapping for each sample.</p
These are the raw data from the DRIVE pooled shRNA screen. It contains read counts for 398 cancer c...
An excel file with all the DNA extraction data which was collected over the course of my study. Incl...
Number of reads aligned, per contig, per individuals. Column one contains contig name, column two le...
<p>DNA yields and numbers of genomes inferred from data on ribosomal gene copies.</p
<p>The number of samples for the identification of DNA methylation patterns and differentially methy...
Count matrices and meta data tables from simulated and real world immune cell single-cell RNA-seq ex...
See S1 Table for details. Sample C was sequenced in the presence of control DNA (“DNA CS” from Oxfor...
<p>The number of reads from the isolate that link all alleles in the sequence.</p
<p>Read numbers of sequences obtained from multiplexed samples using adult poly A+ RNA.</p
This contains all tables we generated from RNAseq libraries as read counts as well as statistic resu...
Raw read counts of the transcripts (length is also given) in the different libraries of the RNA-Seq....
SampleID: Name of samplesReadcount: Number of reads for each sample after decontamination of human r...
<p>Number of samples and percentage of samples identified using DNA barcoding, photo identification ...
<p>Number of analyzed RNA and DNA sequences in the study (after alignment to Galgal4).</p
<p>Number of reads after each step of processing and taxonomy mapping for each sample.</p
These are the raw data from the DRIVE pooled shRNA screen. It contains read counts for 398 cancer c...
An excel file with all the DNA extraction data which was collected over the course of my study. Incl...
Number of reads aligned, per contig, per individuals. Column one contains contig name, column two le...
<p>DNA yields and numbers of genomes inferred from data on ribosomal gene copies.</p
<p>The number of samples for the identification of DNA methylation patterns and differentially methy...
Count matrices and meta data tables from simulated and real world immune cell single-cell RNA-seq ex...
See S1 Table for details. Sample C was sequenced in the presence of control DNA (“DNA CS” from Oxfor...
<p>The number of reads from the isolate that link all alleles in the sequence.</p
<p>Read numbers of sequences obtained from multiplexed samples using adult poly A+ RNA.</p
This contains all tables we generated from RNAseq libraries as read counts as well as statistic resu...
Raw read counts of the transcripts (length is also given) in the different libraries of the RNA-Seq....
SampleID: Name of samplesReadcount: Number of reads for each sample after decontamination of human r...
<p>Number of samples and percentage of samples identified using DNA barcoding, photo identification ...
<p>Number of analyzed RNA and DNA sequences in the study (after alignment to Galgal4).</p
<p>Number of reads after each step of processing and taxonomy mapping for each sample.</p
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