To generate an imperial eagle genome assembly, we conducted one lane of paired-end (PE) sequencing and one lane of mate-paired (MP) sequencing using an Illumina HiSeq2500 that produced read lengths of 100 bp. We used Trimmomatic 0.35 to remove adaptors and discard low quality bases as in Doyle et al. (2018). We then used ABySS 1.5.2 to conduct several preliminary assemblies of PE and MP reads, using k-mer lengths ranging from 41 to 61. MP reads were used only during the scaffolding step and a minimum of 10 pairs of reads were required to join two contigs. We determined that a k-mer length of 61 produced the best assembly by considering both N50 values and the length of the longest scaffold
Motivation: The boost of next-generation sequencing technologies provides us with an unprecedented o...
Next Generation Sequencing (NGS) is a disruptive technology that has found widespread acceptance in ...
We have constructed and sequenced several 454 paired end LT libraries with 3 Kb insert size to asses...
The golden eagle genome was assembled in ABySS with the following parameters: abyss-pe s=202 n=10 k=...
New sequencing technology has dramatically altered the landscape of whole-genome sequencing, allowin...
The Falco mexicanus draft genome was generated from paired-end, mate-paired and long reads using ABy...
Researchers have assembled thousands of eukaryotic genomes using Illumina reads, but traditional mat...
Motivation: DNA sequence reads from Sanger and pyrosequencing platforms differ in cost, accuracy, ty...
assembly of complex mammal genomes. One important solution is to use paired-end (PE) sequence infor...
Researchers have assembled thousands of eukaryotic genomes using Illumina reads, but traditional mat...
Background The ability to generate long sequencing reads and access long-range linkage information i...
Long-range and highly accurate de novo assembly from short-read data is one of the most pressing cha...
De novo genome assembly is a fundamental problem in genomics research. When assembling large genomes...
Imperial eagle scaffolds greater than 10 kb were annotated using the MAKER 2.31.9 pipeline. Briefly,...
Many genomes have been sequenced to high-quality draft status using Sanger capillary electrophoresis...
Motivation: The boost of next-generation sequencing technologies provides us with an unprecedented o...
Next Generation Sequencing (NGS) is a disruptive technology that has found widespread acceptance in ...
We have constructed and sequenced several 454 paired end LT libraries with 3 Kb insert size to asses...
The golden eagle genome was assembled in ABySS with the following parameters: abyss-pe s=202 n=10 k=...
New sequencing technology has dramatically altered the landscape of whole-genome sequencing, allowin...
The Falco mexicanus draft genome was generated from paired-end, mate-paired and long reads using ABy...
Researchers have assembled thousands of eukaryotic genomes using Illumina reads, but traditional mat...
Motivation: DNA sequence reads from Sanger and pyrosequencing platforms differ in cost, accuracy, ty...
assembly of complex mammal genomes. One important solution is to use paired-end (PE) sequence infor...
Researchers have assembled thousands of eukaryotic genomes using Illumina reads, but traditional mat...
Background The ability to generate long sequencing reads and access long-range linkage information i...
Long-range and highly accurate de novo assembly from short-read data is one of the most pressing cha...
De novo genome assembly is a fundamental problem in genomics research. When assembling large genomes...
Imperial eagle scaffolds greater than 10 kb were annotated using the MAKER 2.31.9 pipeline. Briefly,...
Many genomes have been sequenced to high-quality draft status using Sanger capillary electrophoresis...
Motivation: The boost of next-generation sequencing technologies provides us with an unprecedented o...
Next Generation Sequencing (NGS) is a disruptive technology that has found widespread acceptance in ...
We have constructed and sequenced several 454 paired end LT libraries with 3 Kb insert size to asses...