<p>Human chr21 (34.2 Mb), Total error rate = 1.0%</p><p>We varied the average read length from 100 to 300 bp and assembled human chromosome 21 at 11.25x and 20.0x coverage to assess the impact of read length on assembly quality. At read lengths of 100–150 bp we observed lower levels of sequence coverage and smaller contig sizes. With 200 bp we achieved good draft coverage with large contig sizes and few misassemblies. Increasing the read length further to 250 bp yielded significant gains while 300 bp did not provide much additional improvement. Interestingly, keeping the read length constant at 200 bp and increasing the coverage from 11.25x to 20.0x produced greater assembly quality gains than increasing the read length from 200 to 300 bp.<...
We have constructed and sequenced several 454 paired end LT libraries with 3 Kb insert size to asses...
Transcriptome assembly using RNA-seq data - particularly in non-model organisms has been dramaticall...
De novo genome assembly is a fundamental problem in genomics research. When assembling large genomes...
<p>Read length = 200 bp, Cov<sub>G</sub> = 10.0x, Cov<sub>R</sub> = 2.0x.</p><p>For human chromosome...
<p>Read length = 200 bp, Total error rate = 1.0%</p><p>We assembled the whole genome of <i>D. melano...
The sequence and assembly of human genomes using long-read sequencing technologies has revolutionize...
New sequencing technology has dramatically altered the landscape of whole-genome sequencing, allowin...
Obtaining the DNA sequence of an entire genome requires the computer assembly of many small segments...
<p>Higher 20.0x coverage levels are shown in bold. A point (<i>x</i>, <i>y</i>) on the graph indicat...
Recent advances in DNA sequencing technology and their focal role in Genome Wide Association Studies...
<p>A) <i>De novo</i> assemblies of 75×2 bp paired end reads (insert size 150–300 bp). B) Scaffolding...
<p><b>A</b>: NG(X) contig length for full and down-sampled coverage data sets. This metric represent...
We report the sequencing and assembly of a reference genome for the human GM12878 Utah/Ceph cell lin...
<p>The paternal and maternal genomes differes in 1% SNPs. The mean insert size is 250bp with 25bp st...
With the reduction in the cost of next-generation sequencing, whole-genome sequencing (WGS)–based me...
We have constructed and sequenced several 454 paired end LT libraries with 3 Kb insert size to asses...
Transcriptome assembly using RNA-seq data - particularly in non-model organisms has been dramaticall...
De novo genome assembly is a fundamental problem in genomics research. When assembling large genomes...
<p>Read length = 200 bp, Cov<sub>G</sub> = 10.0x, Cov<sub>R</sub> = 2.0x.</p><p>For human chromosome...
<p>Read length = 200 bp, Total error rate = 1.0%</p><p>We assembled the whole genome of <i>D. melano...
The sequence and assembly of human genomes using long-read sequencing technologies has revolutionize...
New sequencing technology has dramatically altered the landscape of whole-genome sequencing, allowin...
Obtaining the DNA sequence of an entire genome requires the computer assembly of many small segments...
<p>Higher 20.0x coverage levels are shown in bold. A point (<i>x</i>, <i>y</i>) on the graph indicat...
Recent advances in DNA sequencing technology and their focal role in Genome Wide Association Studies...
<p>A) <i>De novo</i> assemblies of 75×2 bp paired end reads (insert size 150–300 bp). B) Scaffolding...
<p><b>A</b>: NG(X) contig length for full and down-sampled coverage data sets. This metric represent...
We report the sequencing and assembly of a reference genome for the human GM12878 Utah/Ceph cell lin...
<p>The paternal and maternal genomes differes in 1% SNPs. The mean insert size is 250bp with 25bp st...
With the reduction in the cost of next-generation sequencing, whole-genome sequencing (WGS)–based me...
We have constructed and sequenced several 454 paired end LT libraries with 3 Kb insert size to asses...
Transcriptome assembly using RNA-seq data - particularly in non-model organisms has been dramaticall...
De novo genome assembly is a fundamental problem in genomics research. When assembling large genomes...