full genome sequences Search Results


90
BGI Shenzhen full-length hbv genome sequences pthbv2
Full Length Hbv Genome Sequences Pthbv2, supplied by BGI Shenzhen, 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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MGI Tech Co Ltd amplicon-based mpox viral full-length genome sequencing
Phylogenetic analysis of monkeypox <t>(mpox)</t> virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Amplicon Based Mpox Viral Full Length Genome Sequencing, supplied by MGI Tech Co Ltd, 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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Knome Inc full genomic sequence
Phylogenetic analysis of monkeypox <t>(mpox)</t> virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Full Genomic Sequence, supplied by Knome 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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full genomic sequence - by Bioz Stars, 2026-05
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Kazusa Genome Technologies full-length pml orf tagged with a halo-tag sequence at the n-terminus
Phylogenetic analysis of monkeypox <t>(mpox)</t> virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Full Length Pml Orf Tagged With A Halo Tag Sequence At The N Terminus, supplied by Kazusa Genome Technologies, 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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Sure Genomics full genomic sequencing and testing
Phylogenetic analysis of monkeypox <t>(mpox)</t> virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Full Genomic Sequencing And Testing, supplied by Sure Genomics, 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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full genomic sequencing and testing - by Bioz Stars, 2026-05
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Broad Institute Inc full-length sequences of viral rna genomes
Phylogenetic analysis of monkeypox <t>(mpox)</t> virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Full Length Sequences Of Viral Rna Genomes, supplied by Broad Institute 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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Oxford Nanopore capturing structural variants of herpes simplex virus genome in full length by oxford nanopore sequencing
Phylogenetic analysis of monkeypox <t>(mpox)</t> virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Capturing Structural Variants Of Herpes Simplex Virus Genome In Full Length By Oxford Nanopore Sequencing, supplied by Oxford Nanopore, 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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capturing structural variants of herpes simplex virus genome in full length by oxford nanopore sequencing - by Bioz Stars, 2026-05
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iGeneTech Bioscience Co Ltd customized panel of probes that cover the full-length antisense emcv genomic sequence
Phylogenetic analysis of monkeypox <t>(mpox)</t> virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Customized Panel Of Probes That Cover The Full Length Antisense Emcv Genomic Sequence, supplied by iGeneTech Bioscience Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/customized panel of probes that cover the full-length antisense emcv genomic sequence/product/iGeneTech Bioscience Co Ltd
Average 90 stars, based on 1 article reviews
customized panel of probes that cover the full-length antisense emcv genomic sequence - by Bioz Stars, 2026-05
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Microsynth ag pcr amplification and sanger sequencing of the full-length genomic integration fragment
Phylogenetic analysis of monkeypox <t>(mpox)</t> virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Pcr Amplification And Sanger Sequencing Of The Full Length Genomic Integration Fragment, supplied by Microsynth ag, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/pcr amplification and sanger sequencing of the full-length genomic integration fragment/product/Microsynth ag
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pcr amplification and sanger sequencing of the full-length genomic integration fragment - by Bioz Stars, 2026-05
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ANSES laboratories full-genome sequences
Phylogenetic analysis of monkeypox <t>(mpox)</t> virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Full Genome Sequences, supplied by ANSES laboratories, 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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full-genome sequences - by Bioz Stars, 2026-05
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Loop Genomics 16s full-length-based synthetic long-read sequencing (sfl16s)
Comparison of bacterial taxonomy classification according to two different <t>16S</t> amplicon regions. ( a ) The Venn-diagram is divided into two different methods (red: V3-V4 amplicon and blue: sFL16S) and shows the number of a classified bacterial taxon at the phylum to species level. ( b ) The heatmap shows the frequency of the only identified taxa in both methods drawn by each taxonomic rank, in order. The bacterial taxon belonging to the four major phyla ( Bacteroidetes , Firmicutes , Actinobacteria , and Proteobacteria ), to the species, showing the confidence score of each taxon. The darkness of the color is proportional to the confidence score's value, as shown in the color bar.
16s Full Length Based Synthetic Long Read Sequencing (Sfl16s), supplied by Loop Genomics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/16s full-length-based synthetic long-read sequencing (sfl16s)/product/Loop Genomics
Average 90 stars, based on 1 article reviews
16s full-length-based synthetic long-read sequencing (sfl16s) - by Bioz Stars, 2026-05
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Kazusa Genome Technologies full-length human p63 cdna sequence
Comparison of bacterial taxonomy classification according to two different <t>16S</t> amplicon regions. ( a ) The Venn-diagram is divided into two different methods (red: V3-V4 amplicon and blue: sFL16S) and shows the number of a classified bacterial taxon at the phylum to species level. ( b ) The heatmap shows the frequency of the only identified taxa in both methods drawn by each taxonomic rank, in order. The bacterial taxon belonging to the four major phyla ( Bacteroidetes , Firmicutes , Actinobacteria , and Proteobacteria ), to the species, showing the confidence score of each taxon. The darkness of the color is proportional to the confidence score's value, as shown in the color bar.
Full Length Human P63 Cdna Sequence, supplied by Kazusa Genome Technologies, 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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Image Search Results


Phylogenetic analysis of monkeypox (mpox) virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Journal: Biosafety and Health

Article Title: Molecular phylogenomic analysis reveals a single origin of monkeypox virus transmission in Guangzhou, China in June 2023

doi: 10.1016/j.bsheal.2023.08.002

Figure Lengend Snippet: Phylogenetic analysis of monkeypox (mpox) virus sequences first reported in Guangzhou, China. A) The eight local sequences (red dot) in FASTA format were aligned by the BioEdit software 7.0.9 with the reference sequences of mpox viral clade IIb downloaded from GISAID (black dot) and NCBI (NC_063383.1, green dot, selected as the outgroup). The maximum likelihood (ML) phylogenetic tree of the full-length genome sequences of mpox virus was constructed with the MEGA software 11.0.11 using the General Time Reversible model with 500 bootstrap replicates. The scale bar represents the genetic distance. Bootstrap values >75% are presented at the corresponding nodes of the tree. Abbreviations: FASTA, Fast-All; GISAID, Global Initiative on Sharing Avian Influenza Data; NCBI, National Center For Biotechnology Information. B) The analysis of amino acid mutation of the eight local sequences compared to the reference Japan|EPI ISL 17692269|2023-04-28. In most cases, the mutation sites are mixed. Only the dominant amino acid is shown. “*” represents termination codon. As for this special site, the CAG (Q) codon accounts for 29.26% of all reads, but the TAG (stop) codon accounts for 70.74%. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Article Snippet: We then performed the amplicon-based mpox viral full-length genome sequencing of mpox virus using a newly developed method by MGI Tech Co., Ltd. (MGI), China.

Techniques: Virus, Software, Construct, Mutagenesis

Comparison of bacterial taxonomy classification according to two different 16S amplicon regions. ( a ) The Venn-diagram is divided into two different methods (red: V3-V4 amplicon and blue: sFL16S) and shows the number of a classified bacterial taxon at the phylum to species level. ( b ) The heatmap shows the frequency of the only identified taxa in both methods drawn by each taxonomic rank, in order. The bacterial taxon belonging to the four major phyla ( Bacteroidetes , Firmicutes , Actinobacteria , and Proteobacteria ), to the species, showing the confidence score of each taxon. The darkness of the color is proportional to the confidence score's value, as shown in the color bar.

Journal: Scientific Reports

Article Title: The effect of taxonomic classification by full-length 16S rRNA sequencing with a synthetic long-read technology

doi: 10.1038/s41598-020-80826-9

Figure Lengend Snippet: Comparison of bacterial taxonomy classification according to two different 16S amplicon regions. ( a ) The Venn-diagram is divided into two different methods (red: V3-V4 amplicon and blue: sFL16S) and shows the number of a classified bacterial taxon at the phylum to species level. ( b ) The heatmap shows the frequency of the only identified taxa in both methods drawn by each taxonomic rank, in order. The bacterial taxon belonging to the four major phyla ( Bacteroidetes , Firmicutes , Actinobacteria , and Proteobacteria ), to the species, showing the confidence score of each taxon. The darkness of the color is proportional to the confidence score's value, as shown in the color bar.

Article Snippet: Loop Genomics recently proposed a new 16S full-length-based synthetic long-read sequencing technology (sFL16S).

Techniques: Comparison, Amplification

Phylogenetic tree analysis based on distance matrix calculated by multiple sequence alignment (MSA). ( a ) Neighbor-joining phylogenetic tree analysis of the Bifidobacterium strains identified in both methods. The 16S reference sequences were obtained from the SILVA 138v non-redundant ribosomal RNA gene database. The pink, orange, and green boxes indicate the clustered ASVs by Bifidobacterium species. ( b ) MSA with the reference sequence for the Bifidobacterium strains and ASVs identified from V3V4 and sFL16S. The alignment analysis was performed by the IUB multiple alignment matrix with options (transition weight 0.50; delay-divergent cutoff 30%) using MEGA X software. The MSA results visualized using the NCBI Multiple Sequence Alignment Viewer 1.16.1v.

Journal: Scientific Reports

Article Title: The effect of taxonomic classification by full-length 16S rRNA sequencing with a synthetic long-read technology

doi: 10.1038/s41598-020-80826-9

Figure Lengend Snippet: Phylogenetic tree analysis based on distance matrix calculated by multiple sequence alignment (MSA). ( a ) Neighbor-joining phylogenetic tree analysis of the Bifidobacterium strains identified in both methods. The 16S reference sequences were obtained from the SILVA 138v non-redundant ribosomal RNA gene database. The pink, orange, and green boxes indicate the clustered ASVs by Bifidobacterium species. ( b ) MSA with the reference sequence for the Bifidobacterium strains and ASVs identified from V3V4 and sFL16S. The alignment analysis was performed by the IUB multiple alignment matrix with options (transition weight 0.50; delay-divergent cutoff 30%) using MEGA X software. The MSA results visualized using the NCBI Multiple Sequence Alignment Viewer 1.16.1v.

Article Snippet: Loop Genomics recently proposed a new 16S full-length-based synthetic long-read sequencing technology (sFL16S).

Techniques: Sequencing, Software

Comparison of taxonomy matching accuracy for V3V4 and sFL16S on NCBI Bacterial Genome Database. Violin plots represent matching rates that result from taxonomy matching analysis in the NCBI Bacterial Genome Database (40 K bacterial and archaeal genomes), according to taxonomic rank (genus and species). Using the NCBI reference 16S sequence data, we conducted the BLAST search to determine the matching rate with the ASV taxonomy data in two different methods. The y-axis indicates the percentiles of the taxonomy matching rate. The violin plots are filled in red (left) and blue (right) for V3V4 and sFL16S data, respectively. The boxes indicate the mean value (black bold horizontal line), percentiles of the taxonomy matching rate distribution. The upper and low whiskers indicate the maximum and the minimum value of the taxonomy matching rate, respectively. The shaded area surrounding the boxes on each side indicate the ASV frequency of the taxonomy matching rate.

Journal: Scientific Reports

Article Title: The effect of taxonomic classification by full-length 16S rRNA sequencing with a synthetic long-read technology

doi: 10.1038/s41598-020-80826-9

Figure Lengend Snippet: Comparison of taxonomy matching accuracy for V3V4 and sFL16S on NCBI Bacterial Genome Database. Violin plots represent matching rates that result from taxonomy matching analysis in the NCBI Bacterial Genome Database (40 K bacterial and archaeal genomes), according to taxonomic rank (genus and species). Using the NCBI reference 16S sequence data, we conducted the BLAST search to determine the matching rate with the ASV taxonomy data in two different methods. The y-axis indicates the percentiles of the taxonomy matching rate. The violin plots are filled in red (left) and blue (right) for V3V4 and sFL16S data, respectively. The boxes indicate the mean value (black bold horizontal line), percentiles of the taxonomy matching rate distribution. The upper and low whiskers indicate the maximum and the minimum value of the taxonomy matching rate, respectively. The shaded area surrounding the boxes on each side indicate the ASV frequency of the taxonomy matching rate.

Article Snippet: Loop Genomics recently proposed a new 16S full-length-based synthetic long-read sequencing technology (sFL16S).

Techniques: Comparison, Sequencing

Comparison of the taxon matching rate with NCBI bacterial genome database.

Journal: Scientific Reports

Article Title: The effect of taxonomic classification by full-length 16S rRNA sequencing with a synthetic long-read technology

doi: 10.1038/s41598-020-80826-9

Figure Lengend Snippet: Comparison of the taxon matching rate with NCBI bacterial genome database.

Article Snippet: Loop Genomics recently proposed a new 16S full-length-based synthetic long-read sequencing technology (sFL16S).

Techniques: Comparison