Abstract Background Transposome-based technologies have enabled the streamlined production of sequencer-ready DNA libraries; however, current methods are highly sensitive to the amount and quality of input nucleic acid. Results We describe a new library preparation technology (Nextera DNA Flex) that utilizes a known concentration of transposomes conjugated directly to beads to bind a fixed amount of DNA, and enables direct input of blood and saliva using an integrated extraction protocol. We further report results from libraries generated outside the standard parameters of the workflow, highlighting novel applications for Nextera DNA Flex, including human genome builds and variant calling from below 1 ng DNA input, customization of insert s...
<div><p>Next-generation sequencing (NGS) is emerging as a powerful tool for elucidating genetic info...
Tumor DNA sequencing results can have important clinical implications. However, its use is often lim...
High-throughput preparation of plasmid DNA libraries for next-generation sequencing (NGS) is an impo...
Abstract Background Next-gener...
BACKGROUND: The Nextera protocol, which utilises a transposome based approach to create libraries fo...
New sequencing technologies can address diverse biomedical questions but are limited by a minimum re...
Massively parallel sequencing systems continue to improve on data output, while leaving labor-intens...
Abstract Background For next generation DNA sequencing, we have developed a rapid and simple approac...
BackgroundCell-free DNA (cfDNA), present in circulating blood plasma, contains information about pre...
Background: Genomic testing is often limited by the exhaustible nature of human tissue and blood sam...
Efficient preparation of high-quality sequencing libraries that well represent the biological sample...
Abstract Background Next-generation sequencing (NGS) has revolutionized almost all fields of biology...
Construction of DNA fragment libraries for next-generation sequencing can prove challenging, especia...
High-throughput sequencing, also known as next-generation sequencing (NGS), has revolutionized genom...
Construction of DNA fragment libraries for next-generation sequencing can prove challenging, especia...
<div><p>Next-generation sequencing (NGS) is emerging as a powerful tool for elucidating genetic info...
Tumor DNA sequencing results can have important clinical implications. However, its use is often lim...
High-throughput preparation of plasmid DNA libraries for next-generation sequencing (NGS) is an impo...
Abstract Background Next-gener...
BACKGROUND: The Nextera protocol, which utilises a transposome based approach to create libraries fo...
New sequencing technologies can address diverse biomedical questions but are limited by a minimum re...
Massively parallel sequencing systems continue to improve on data output, while leaving labor-intens...
Abstract Background For next generation DNA sequencing, we have developed a rapid and simple approac...
BackgroundCell-free DNA (cfDNA), present in circulating blood plasma, contains information about pre...
Background: Genomic testing is often limited by the exhaustible nature of human tissue and blood sam...
Efficient preparation of high-quality sequencing libraries that well represent the biological sample...
Abstract Background Next-generation sequencing (NGS) has revolutionized almost all fields of biology...
Construction of DNA fragment libraries for next-generation sequencing can prove challenging, especia...
High-throughput sequencing, also known as next-generation sequencing (NGS), has revolutionized genom...
Construction of DNA fragment libraries for next-generation sequencing can prove challenging, especia...
<div><p>Next-generation sequencing (NGS) is emerging as a powerful tool for elucidating genetic info...
Tumor DNA sequencing results can have important clinical implications. However, its use is often lim...
High-throughput preparation of plasmid DNA libraries for next-generation sequencing (NGS) is an impo...