This is the software described in paper "SynthEx: A synthetic-normal based DNA sequencing tool for copy number alteration detection and tumor heterogeneity profiling. Grace O. Silva, Marni B. Siegel, Lisle E. Mose, Joel S. Parker, Wei Sun, Charles M. Perou and Mengjie Chen". This release made the following changes: The input and output BED files are now 0-based. Add the output of bin level log2 ratio
Scientific and technological advances in recent decades have significantly altered the nature of bio...
Recent advances in high-throughput sequencing (HTS) technologies and computing capacity have produce...
In January 2022, our institution launched a comprehensive cancer genome profiling program on 10 canc...
This is the software described in paper "SynthEx: A synthetic-normal based DNA sequencing tool for c...
Abstract Changes in the quantity of genetic material, known as somatic copy number alterations (CNAs...
TCGA head and neck squamous cell carcinoma clinical information of tumors used in comparisons (nâ=...
As next-generation sequencing technology advances and the cost decreases, whole genome sequencing (W...
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...
Genomic copy number alterations (CNA) and loss of heterozygozity (LOH) are two types of genomic inst...
Summary: GeneContent is a software system to infer the genome phylogeny based on an additive genome ...
WhatsHap is a software for phasing genomic variants using DNA sequencing reads, also called haplotyp...
The Human Genome Project focuses on identifying and mapping human genome genes and the base pair of ...
Massive parallel sequencing is a powerful tool for variant discovery and genotyping. To reduce costs...
Copyright © 2012 Chun-Tien Chang et al. This is an open access article distributed under the Creativ...
International audienceWe describe a method for automatic detection of absolute segmental copy number...
Scientific and technological advances in recent decades have significantly altered the nature of bio...
Recent advances in high-throughput sequencing (HTS) technologies and computing capacity have produce...
In January 2022, our institution launched a comprehensive cancer genome profiling program on 10 canc...
This is the software described in paper "SynthEx: A synthetic-normal based DNA sequencing tool for c...
Abstract Changes in the quantity of genetic material, known as somatic copy number alterations (CNAs...
TCGA head and neck squamous cell carcinoma clinical information of tumors used in comparisons (nâ=...
As next-generation sequencing technology advances and the cost decreases, whole genome sequencing (W...
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...
Genomic copy number alterations (CNA) and loss of heterozygozity (LOH) are two types of genomic inst...
Summary: GeneContent is a software system to infer the genome phylogeny based on an additive genome ...
WhatsHap is a software for phasing genomic variants using DNA sequencing reads, also called haplotyp...
The Human Genome Project focuses on identifying and mapping human genome genes and the base pair of ...
Massive parallel sequencing is a powerful tool for variant discovery and genotyping. To reduce costs...
Copyright © 2012 Chun-Tien Chang et al. This is an open access article distributed under the Creativ...
International audienceWe describe a method for automatic detection of absolute segmental copy number...
Scientific and technological advances in recent decades have significantly altered the nature of bio...
Recent advances in high-throughput sequencing (HTS) technologies and computing capacity have produce...
In January 2022, our institution launched a comprehensive cancer genome profiling program on 10 canc...
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