Next-generation sequencing has proven an ex-tremely effective technology for molecular counting applications where the number of sequence reads provides a digital readout for RNA-seq, ChIP-seq, Tn-seq and other applications. The extremely large number of sequence reads that can be obtained per run permits the analysis of increasingly complex samples. For lower complexity samples, however, a point of diminishing returns is reached when the number of counts per sequence results in oversampling with no increase in data quality. A solution to making next-generation sequencing as efficient and affordable as possible involves assaying multiple samples in a single run
Next-generation sequencing (NGS) is a powerful tool for analyzing environmental DNA and provides the...
The work presented in this thesis describes methodologies developed for integration and accurate int...
Abstract — Huge efforts are being made to develop algorithms and procedures for DNA sequences. The p...
Abstract Background The multiplexing becomes the major limitation of the next-generation sequencing ...
Next-generation sequencers have sufficient power to analyze simultaneously DNAs from many different ...
Short DNA oligonucleotides (~4 mer) have been used to index samples from different sources, such as ...
The use and validation of a strategy that allows a universal set of bar-coded sequencing primers to ...
Short DNA oligonucleotides (~4 mer) have been used to index samples from different sources, such as ...
Synthetic DNA barcodes are double-stranded DNA molecules designed to carry recoverable information, ...
DNA barcoding is an efficient method to identify specimens and to detect undescribed/cryptic species...
The diversity and scope of multiplex parallel sequencing applications is steadily increasing. Critic...
Although different instruments for massively parallel sequencing exist, each with their own chemistr...
Abstract Barcoding technology has greatly improved the throughput of cells and genes detected in sin...
The diversity and scope of multiplex parallel sequencing applications is steadily increasing. Critic...
The diversity and scope of multiplex parallel sequencing applications is steadily increasing. Critic...
Next-generation sequencing (NGS) is a powerful tool for analyzing environmental DNA and provides the...
The work presented in this thesis describes methodologies developed for integration and accurate int...
Abstract — Huge efforts are being made to develop algorithms and procedures for DNA sequences. The p...
Abstract Background The multiplexing becomes the major limitation of the next-generation sequencing ...
Next-generation sequencers have sufficient power to analyze simultaneously DNAs from many different ...
Short DNA oligonucleotides (~4 mer) have been used to index samples from different sources, such as ...
The use and validation of a strategy that allows a universal set of bar-coded sequencing primers to ...
Short DNA oligonucleotides (~4 mer) have been used to index samples from different sources, such as ...
Synthetic DNA barcodes are double-stranded DNA molecules designed to carry recoverable information, ...
DNA barcoding is an efficient method to identify specimens and to detect undescribed/cryptic species...
The diversity and scope of multiplex parallel sequencing applications is steadily increasing. Critic...
Although different instruments for massively parallel sequencing exist, each with their own chemistr...
Abstract Barcoding technology has greatly improved the throughput of cells and genes detected in sin...
The diversity and scope of multiplex parallel sequencing applications is steadily increasing. Critic...
The diversity and scope of multiplex parallel sequencing applications is steadily increasing. Critic...
Next-generation sequencing (NGS) is a powerful tool for analyzing environmental DNA and provides the...
The work presented in this thesis describes methodologies developed for integration and accurate int...
Abstract — Huge efforts are being made to develop algorithms and procedures for DNA sequences. The p...