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Data set 1 was of constant 30-fold coverage. Data set 2 and 3 were of varying coverage. Data set 1 and 2 were generated with the default read length distribution of ART whereas data set 3 was generated with a customized longer read length distribution. If there are repeated k-mers in sequence or all the k-mers are isolated in the <t>de</t> <t>Bruijn</t> graph, then this read is defined as “useless” here.
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Data set 1 was of constant 30-fold coverage. Data set 2 and 3 were of varying coverage. Data set 1 and 2 were generated with the default read length distribution of ART whereas data set 3 was generated with a customized longer read length distribution. If there are repeated k-mers in sequence or all the k-mers are isolated in the <t>de</t> <t>Bruijn</t> graph, then this read is defined as “useless” here.
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Illumina Inc de bruijn assembly graph
Data set 1 was of constant 30-fold coverage. Data set 2 and 3 were of varying coverage. Data set 1 and 2 were generated with the default read length distribution of ART whereas data set 3 was generated with a customized longer read length distribution. If there are repeated k-mers in sequence or all the k-mers are isolated in the <t>de</t> <t>Bruijn</t> graph, then this read is defined as “useless” here.
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Illumina Inc de-bruijn graph-based trinity assembler
Data set 1 was of constant 30-fold coverage. Data set 2 and 3 were of varying coverage. Data set 1 and 2 were generated with the default read length distribution of ART whereas data set 3 was generated with a customized longer read length distribution. If there are repeated k-mers in sequence or all the k-mers are isolated in the <t>de</t> <t>Bruijn</t> graph, then this read is defined as “useless” here.
De Bruijn Graph Based Trinity Assembler, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Illumina Inc de bruijn graph
Overview of the Ultraplexing approach. Long reads are generated in simple pooled sequencing runs. The Ultraplexing algorithm determines the most likely source genome for each long read by carrying out a comparison between the read and the <t>de</t> <t>Bruijn</t> graphs of the sequenced sample genomes, inferred from short-read data. Hybrid assembly of sample-specific long and short reads enables the recovery of complete bacterial genomes
De Bruijn Graph, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Data set 1 was of constant 30-fold coverage. Data set 2 and 3 were of varying coverage. Data set 1 and 2 were generated with the default read length distribution of ART whereas data set 3 was generated with a customized longer read length distribution. If there are repeated k-mers in sequence or all the k-mers are isolated in the de Bruijn graph, then this read is defined as “useless” here.

Journal: PLoS ONE

Article Title: Evaluating de Bruijn Graph Assemblers on 454 Transcriptomic Data

doi: 10.1371/journal.pone.0051188

Figure Lengend Snippet: Data set 1 was of constant 30-fold coverage. Data set 2 and 3 were of varying coverage. Data set 1 and 2 were generated with the default read length distribution of ART whereas data set 3 was generated with a customized longer read length distribution. If there are repeated k-mers in sequence or all the k-mers are isolated in the de Bruijn graph, then this read is defined as “useless” here.

Article Snippet: In this study, we conducted such an evaluation and found that those Illumina/Solexa-specialized de Bruijn graph assemblers performed well on 454 transcriptomic data.

Techniques: Generated, Sequencing, Isolation

Overview of the Ultraplexing approach. Long reads are generated in simple pooled sequencing runs. The Ultraplexing algorithm determines the most likely source genome for each long read by carrying out a comparison between the read and the de Bruijn graphs of the sequenced sample genomes, inferred from short-read data. Hybrid assembly of sample-specific long and short reads enables the recovery of complete bacterial genomes

Journal: Genome Biology

Article Title: Ultraplexing: increasing the efficiency of long-read sequencing for hybrid assembly with k -mer-based multiplexing

doi: 10.1186/s13059-020-01974-9

Figure Lengend Snippet: Overview of the Ultraplexing approach. Long reads are generated in simple pooled sequencing runs. The Ultraplexing algorithm determines the most likely source genome for each long read by carrying out a comparison between the read and the de Bruijn graphs of the sequenced sample genomes, inferred from short-read data. Hybrid assembly of sample-specific long and short reads enables the recovery of complete bacterial genomes

Article Snippet: For each sample, a de Bruijn graph ( k = 19) is constructed from the sample-specific Illumina short-read data and the graph is cleaned (removal of low-coverage supernodes) with Cortex [ ].

Techniques: Generated, Sequencing, Comparison