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Alignment for Next-Generation Sequencing Data
, 2014
"... HIVE-hexagon: High-performance, parallelized sequence alignment for next-generation sequencing data analysis ..."
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HIVE-hexagon: High-performance, parallelized sequence alignment for next-generation sequencing data analysis
of next-generation sequencing data
, 2011
"... Motivation: The growth of next-generation sequencing means that more effective and efficient archiving methods are needed to store the generated data for public dissemination and in anticipation of more mature analytical methods later. This article examines methods for compressing the quality score ..."
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Motivation: The growth of next-generation sequencing means that more effective and efficient archiving methods are needed to store the generated data for public dissemination and in anticipation of more mature analytical methods later. This article examines methods for compressing the quality score
Welcome to Next-Generation Sequencing
"... www.illumina.com/NGS Deciphering DNA sequences is essential for virtually all branches of biological research. With the advent of capillary electrophoresis (CE)-based Sanger sequencing, scientists gained the ability to elucidate genetic information from any given biological system. This technology h ..."
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, an entirely new technology was required—Next-Generation Sequencing (NGS), a fundamentally different approach to sequencing that triggered numerous ground-breaking discoveries and ignited a revolution in genomic science.
variations with next-generation sequencing
, 2012
"... Motivation: Analysing next-generation sequencing (NGS) data for copy number variations (CNVs) detection is a relatively new and chal-lenging field, with no accepted standard protocols or quality control measures so far. There are by now several algorithms developed for each of the four broad methods ..."
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Motivation: Analysing next-generation sequencing (NGS) data for copy number variations (CNVs) detection is a relatively new and chal-lenging field, with no accepted standard protocols or quality control measures so far. There are by now several algorithms developed for each of the four broad
Editorial Next-Generation Sequencing
"... It has been widely appreciated that the genome sequence is shaping the future biomedical research. The genome sequence provides a general framework for assembling fragmentary DNA information into landscape of biological structure and function Starting in 2005, a variety of massively parallel seque ..."
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sequences machines share some common remarkable features When sequencing becomes simple and inexpensive, it is being routinely applied to biomedical research. To create comprehensive catalogues of genomic variants, the next-generation sequencing technologies have been used to produce sequence data
Archiving next generation sequencing data,
- Nucleic Acids Research,
, 2010
"... ABSTRACT Next generation sequencing platforms are producing biological sequencing data in unprecedented amounts. ..."
Abstract
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Cited by 28 (4 self)
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ABSTRACT Next generation sequencing platforms are producing biological sequencing data in unprecedented amounts.
Next-generation sequencing in n
"... surgsci.uu.se screening of PCC. The bioinformatics analysis may be performed without expert skills. We Key Words " exome sequencing " whole genome sequencing " pheochromocytoma " paraganglioma ..."
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surgsci.uu.se screening of PCC. The bioinformatics analysis may be performed without expert skills. We Key Words " exome sequencing " whole genome sequencing " pheochromocytoma " paraganglioma
Next-generation Sequencing of U
"... (Table 1), (2) we are confronted with new tumour terised by mutations in chromatin remodellers/PBRM1, Ongoing studies of ccRCC from France and China and the EURO P E AN URO L OGY 6 6 ( 2 0 1 4) 4 – 7 avai lable at www.sciencedirect.com journal homepage: www.europeanurology.com1. Renal cell carcinoma ..."
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carcinomataxonomies, and (3) new opportunities for improved management have arisen. TCGA project on papillary tumours will support a more detailed understanding of renal cell carcinoma (RCC) genomic diversity. 2. Bladder cancercolorectal, breast, and pancreatic cancer using Sanger sequencing. Since 2010, WES and WGS
Next-generation sequencing: a
, 2013
"... challenge to meet the increasing demand for training workshops in ..."
next-generation sequencing data
, 2012
"... PriVar: a toolkit for prioritizing SNVs and indels from ..."
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