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Simplot Science boot scanning analysis simplot v3.5.1
Recombination events and breakpoints identified in NACMR092. (A) Recombinant breakpoint positions were calculated by boot scanning analysis using Simplot <t>v3.5.1,</t> as described. The percentages of permuted trees (y-axis) of the subtypes at each sequence position (x-axis) are shown. (B) Genomic map of the near-full-length sequence of NACMR092 (based on HXB2 numbering). The mosaic map was generated using the Los Alamos Recombinant HIV-1 Drawing Tool (https://hiv.lanl.gov/content/sequence/DRAW_CRF/recom_mapper.html). The start (nucleotide 874) and end (nucleotide 9403) of the near-full-length sequence, as well as the breakpoints are shown. Genomic sequences originating from HIV-1 subtype A1 (grey color), CRF01_AE (red color), and CRF02_AG (blue color) are shown. LTR, long-terminal repeat; gag, group-specific antigen; pol, polymerase; vif, viral infectivity factor; vpr, viral protein R; vpu, viral protein U; env, envelope; tat, trans-activator of transcription; nef, negative factor. Color images are available online.
Boot Scanning Analysis Simplot V3.5.1, supplied by Simplot Science, 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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Average 90 stars, based on 1 article reviews
boot scanning analysis simplot v3.5.1 - by Bioz Stars, 2026-04
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1) Product Images from "Near-Full-Length Genetic Characterization of a Novel HIV-1 Unique Recombinant with Similarities to A1, CRF01_AE, and CRFO2_AG Viruses in Yaoundé, Cameroon"

Article Title: Near-Full-Length Genetic Characterization of a Novel HIV-1 Unique Recombinant with Similarities to A1, CRF01_AE, and CRFO2_AG Viruses in Yaoundé, Cameroon

Journal: AIDS Research and Human Retroviruses

doi: 10.1089/aid.2019.0042

Recombination events and breakpoints identified in NACMR092. (A) Recombinant breakpoint positions were calculated by boot scanning analysis using Simplot v3.5.1, as described. The percentages of permuted trees (y-axis) of the subtypes at each sequence position (x-axis) are shown. (B) Genomic map of the near-full-length sequence of NACMR092 (based on HXB2 numbering). The mosaic map was generated using the Los Alamos Recombinant HIV-1 Drawing Tool (https://hiv.lanl.gov/content/sequence/DRAW_CRF/recom_mapper.html). The start (nucleotide 874) and end (nucleotide 9403) of the near-full-length sequence, as well as the breakpoints are shown. Genomic sequences originating from HIV-1 subtype A1 (grey color), CRF01_AE (red color), and CRF02_AG (blue color) are shown. LTR, long-terminal repeat; gag, group-specific antigen; pol, polymerase; vif, viral infectivity factor; vpr, viral protein R; vpu, viral protein U; env, envelope; tat, trans-activator of transcription; nef, negative factor. Color images are available online.
Figure Legend Snippet: Recombination events and breakpoints identified in NACMR092. (A) Recombinant breakpoint positions were calculated by boot scanning analysis using Simplot v3.5.1, as described. The percentages of permuted trees (y-axis) of the subtypes at each sequence position (x-axis) are shown. (B) Genomic map of the near-full-length sequence of NACMR092 (based on HXB2 numbering). The mosaic map was generated using the Los Alamos Recombinant HIV-1 Drawing Tool (https://hiv.lanl.gov/content/sequence/DRAW_CRF/recom_mapper.html). The start (nucleotide 874) and end (nucleotide 9403) of the near-full-length sequence, as well as the breakpoints are shown. Genomic sequences originating from HIV-1 subtype A1 (grey color), CRF01_AE (red color), and CRF02_AG (blue color) are shown. LTR, long-terminal repeat; gag, group-specific antigen; pol, polymerase; vif, viral infectivity factor; vpr, viral protein R; vpu, viral protein U; env, envelope; tat, trans-activator of transcription; nef, negative factor. Color images are available online.

Techniques Used: Recombinant, Sequencing, Generated, Genomic Sequencing, Infection



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Simplot Science boot scanning analysis simplot v3.5.1
Recombination events and breakpoints identified in NACMR092. (A) Recombinant breakpoint positions were calculated by boot scanning analysis using Simplot <t>v3.5.1,</t> as described. The percentages of permuted trees (y-axis) of the subtypes at each sequence position (x-axis) are shown. (B) Genomic map of the near-full-length sequence of NACMR092 (based on HXB2 numbering). The mosaic map was generated using the Los Alamos Recombinant HIV-1 Drawing Tool (https://hiv.lanl.gov/content/sequence/DRAW_CRF/recom_mapper.html). The start (nucleotide 874) and end (nucleotide 9403) of the near-full-length sequence, as well as the breakpoints are shown. Genomic sequences originating from HIV-1 subtype A1 (grey color), CRF01_AE (red color), and CRF02_AG (blue color) are shown. LTR, long-terminal repeat; gag, group-specific antigen; pol, polymerase; vif, viral infectivity factor; vpr, viral protein R; vpu, viral protein U; env, envelope; tat, trans-activator of transcription; nef, negative factor. Color images are available online.
Boot Scanning Analysis Simplot V3.5.1, supplied by Simplot Science, 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/boot scanning analysis simplot v3.5.1/product/Simplot Science
Average 90 stars, based on 1 article reviews
boot scanning analysis simplot v3.5.1 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Simplot Science boot scanning analysis with simplot v3.5.1
Recombination events and breakpoints identified in NACMR092. (A) Recombinant breakpoint positions were calculated by boot scanning analysis using Simplot <t>v3.5.1,</t> as described. The percentages of permuted trees (y-axis) of the subtypes at each sequence position (x-axis) are shown. (B) Genomic map of the near-full-length sequence of NACMR092 (based on HXB2 numbering). The mosaic map was generated using the Los Alamos Recombinant HIV-1 Drawing Tool (https://hiv.lanl.gov/content/sequence/DRAW_CRF/recom_mapper.html). The start (nucleotide 874) and end (nucleotide 9403) of the near-full-length sequence, as well as the breakpoints are shown. Genomic sequences originating from HIV-1 subtype A1 (grey color), CRF01_AE (red color), and CRF02_AG (blue color) are shown. LTR, long-terminal repeat; gag, group-specific antigen; pol, polymerase; vif, viral infectivity factor; vpr, viral protein R; vpu, viral protein U; env, envelope; tat, trans-activator of transcription; nef, negative factor. Color images are available online.
Boot Scanning Analysis With Simplot V3.5.1, supplied by Simplot Science, 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/boot scanning analysis with simplot v3.5.1/product/Simplot Science
Average 90 stars, based on 1 article reviews
boot scanning analysis with simplot v3.5.1 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

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Recombination events and breakpoints identified in NACMR092. (A) Recombinant breakpoint positions were calculated by boot scanning analysis using Simplot v3.5.1, as described. The percentages of permuted trees (y-axis) of the subtypes at each sequence position (x-axis) are shown. (B) Genomic map of the near-full-length sequence of NACMR092 (based on HXB2 numbering). The mosaic map was generated using the Los Alamos Recombinant HIV-1 Drawing Tool (https://hiv.lanl.gov/content/sequence/DRAW_CRF/recom_mapper.html). The start (nucleotide 874) and end (nucleotide 9403) of the near-full-length sequence, as well as the breakpoints are shown. Genomic sequences originating from HIV-1 subtype A1 (grey color), CRF01_AE (red color), and CRF02_AG (blue color) are shown. LTR, long-terminal repeat; gag, group-specific antigen; pol, polymerase; vif, viral infectivity factor; vpr, viral protein R; vpu, viral protein U; env, envelope; tat, trans-activator of transcription; nef, negative factor. Color images are available online.

Journal: AIDS Research and Human Retroviruses

Article Title: Near-Full-Length Genetic Characterization of a Novel HIV-1 Unique Recombinant with Similarities to A1, CRF01_AE, and CRFO2_AG Viruses in Yaoundé, Cameroon

doi: 10.1089/aid.2019.0042

Figure Lengend Snippet: Recombination events and breakpoints identified in NACMR092. (A) Recombinant breakpoint positions were calculated by boot scanning analysis using Simplot v3.5.1, as described. The percentages of permuted trees (y-axis) of the subtypes at each sequence position (x-axis) are shown. (B) Genomic map of the near-full-length sequence of NACMR092 (based on HXB2 numbering). The mosaic map was generated using the Los Alamos Recombinant HIV-1 Drawing Tool (https://hiv.lanl.gov/content/sequence/DRAW_CRF/recom_mapper.html). The start (nucleotide 874) and end (nucleotide 9403) of the near-full-length sequence, as well as the breakpoints are shown. Genomic sequences originating from HIV-1 subtype A1 (grey color), CRF01_AE (red color), and CRF02_AG (blue color) are shown. LTR, long-terminal repeat; gag, group-specific antigen; pol, polymerase; vif, viral infectivity factor; vpr, viral protein R; vpu, viral protein U; env, envelope; tat, trans-activator of transcription; nef, negative factor. Color images are available online.

Article Snippet: Fragments I, II, III, IV, V, VI, VII, VIII, and IX of the mosaic genome correspond, respectively, to nucleotides 874–1526, 1527–1826, 1827–5029, 5030–5629, 5630–6629, 6630–6862, 6863–8862, 8863–9106, and nucleotides 9107–9403 of the HXB2 genome. fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 2. caption a7 Recombination events and breakpoints identified in NACMR092. (A) Recombinant breakpoint positions were calculated by boot scanning analysis using Simplot v3.5.1, as described.

Techniques: Recombinant, Sequencing, Generated, Genomic Sequencing, Infection