<p>576 DNA samples (S<i><sub>n</sub></i>) were arranged in six 96 well plates. These samples were pooled in 4 matrices of 12 rows by 12 columns as illustrated. For each pool, 12 DNA samples were either pooled across the grid (row) or down the grid (column). Each pool of 12 DNA samples was then target enriched, barcoded and processed for Illumina sequencing.</p
The output from whole genome sequencing is a set of contigs, i.e. short non-overlapping DNA sequence...
BACKGROUND: Solution-based targeted genomic enrichment (TGE) protocols permit selective sequencing o...
The output from whole genome sequencing is a set of contigs, i.e. short non-overlapping DNA sequence...
We describe a method for pooling and sequencing DNA from a large number of individual samples while ...
We describe a method for pooling and sequencing DNA from a large number of individual samples while ...
<p>After sample matching and pool creation, the pools are grouped into <i>K</i> groups, with allele ...
Next-generation sequencers have sufficient power to analyze simultaneously DNAs from many different ...
this excel file shows the pooling of PCR amplicons (38 markers used) for 288 individuals in a 96-wel...
Background: High throughput sequencing is frequently used to discover the location of regulatory int...
<p>(A) Individual viral sequences within a quasispecies are assigned with a unique tag. In this exam...
<p>The raw yield, percentage of reads mapped, percentage of reads on target, the total coverage of t...
<p>A. Workflow of the 2D-PCR pooling B. An example of the pooling design for 16 plants. Each plant g...
Raw Illumina sequence reads for 34 individuals, demultiplexed by individual barcode tags. Within ea...
<div><p>The output from whole genome sequencing is a set of contigs, i.e. short non-overlapping DNA ...
DNA pooling is a practical way to reduce the cost of large-scale association studies to identify sus...
The output from whole genome sequencing is a set of contigs, i.e. short non-overlapping DNA sequence...
BACKGROUND: Solution-based targeted genomic enrichment (TGE) protocols permit selective sequencing o...
The output from whole genome sequencing is a set of contigs, i.e. short non-overlapping DNA sequence...
We describe a method for pooling and sequencing DNA from a large number of individual samples while ...
We describe a method for pooling and sequencing DNA from a large number of individual samples while ...
<p>After sample matching and pool creation, the pools are grouped into <i>K</i> groups, with allele ...
Next-generation sequencers have sufficient power to analyze simultaneously DNAs from many different ...
this excel file shows the pooling of PCR amplicons (38 markers used) for 288 individuals in a 96-wel...
Background: High throughput sequencing is frequently used to discover the location of regulatory int...
<p>(A) Individual viral sequences within a quasispecies are assigned with a unique tag. In this exam...
<p>The raw yield, percentage of reads mapped, percentage of reads on target, the total coverage of t...
<p>A. Workflow of the 2D-PCR pooling B. An example of the pooling design for 16 plants. Each plant g...
Raw Illumina sequence reads for 34 individuals, demultiplexed by individual barcode tags. Within ea...
<div><p>The output from whole genome sequencing is a set of contigs, i.e. short non-overlapping DNA ...
DNA pooling is a practical way to reduce the cost of large-scale association studies to identify sus...
The output from whole genome sequencing is a set of contigs, i.e. short non-overlapping DNA sequence...
BACKGROUND: Solution-based targeted genomic enrichment (TGE) protocols permit selective sequencing o...
The output from whole genome sequencing is a set of contigs, i.e. short non-overlapping DNA sequence...