Review





Similar Products

97
Complete Genomics Inc mgieasy whole genome bisulfite 487 sequencing library prep kit
Mgieasy Whole Genome Bisulfite 487 Sequencing Library Prep Kit, supplied by Complete Genomics Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mgieasy whole genome bisulfite 487 sequencing library prep kit/product/Complete Genomics Inc
Average 97 stars, based on 1 article reviews
mgieasy whole genome bisulfite 487 sequencing library prep kit - by Bioz Stars, 2026-05
97/100 stars
  Buy from Supplier

95
Zymo Research low input msp1 reduced representation bisulfite sequencing rrbs
Low Input Msp1 Reduced Representation Bisulfite Sequencing Rrbs, supplied by Zymo Research, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/low input msp1 reduced representation bisulfite sequencing rrbs/product/Zymo Research
Average 95 stars, based on 1 article reviews
low input msp1 reduced representation bisulfite sequencing rrbs - by Bioz Stars, 2026-05
95/100 stars
  Buy from Supplier

86
Novogene genome bisulfite sequencing
Samples taken from the two MA pedigrees for different experiments. A) Ten MA lines were sampled from the two pedigrees. Samples for <t>sequencing</t> were taken after 5, 20, and 40 transfers and DNA methylation was detected using bisulfite sequencing (red circles). B) Three additional MA lines were sampled from both pedigrees and samples were taken after 1, 5, 7, 8, 10, and 15 transfers for Nanopore sequencing and after 5, 8, 10, 20, and 40 transfers for H3K9me3 ChIP-seq.
Genome Bisulfite Sequencing, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/genome bisulfite sequencing/product/Novogene
Average 86 stars, based on 1 article reviews
genome bisulfite sequencing - by Bioz Stars, 2026-05
86/100 stars
  Buy from Supplier

86
Novogene input whole genome bisulfite sequencing
<t>Whole-genome</t> <t>DNA</t> methylation analysis of Chinese yam variant F2000 and F60. A Principal component 1 and principal component 2 analyses were performed for each sample. B Methylation level distribution across genetic features including 4 kb upstream of TSS, gene body, and 4 kb downstream of TTS in the three DNA methylation contexts CG, CHG, and CHH. Analyses were performed in biological triplicates for each variant. C Number of DMRs with higher methylation levels in F2000 (hypermethylated) and in F60 (hypomethylated). DMRs were investigated in the three DNA methylation contexts CG, CHG and CHH. Distribution of DMRs upstream in the putative promoter (4 kb of TSS), within the gene body, and down-stream in the putative terminator (4 kb of TTS) were analyzed in DMR-associated genes (q-value ≤ 0.01, methylation difference >|10%|). D Venn analysis of DMR-associated genes split in hyper- and hypomethylated promoters, gene bodies, and terminators. DMR, differentially methylated region; TSS, transcription start site; TTS, transcription termination site
Input Whole Genome Bisulfite Sequencing, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/input whole genome bisulfite sequencing/product/Novogene
Average 86 stars, based on 1 article reviews
input whole genome bisulfite sequencing - by Bioz Stars, 2026-05
86/100 stars
  Buy from Supplier

86
Novogene low input whole genome bisulfite sequencing prepared dna
<t>Whole-genome</t> <t>DNA</t> methylation analysis of Chinese yam variant F2000 and F60. A Principal component 1 and principal component 2 analyses were performed for each sample. B Methylation level distribution across genetic features including 4 kb upstream of TSS, gene body, and 4 kb downstream of TTS in the three DNA methylation contexts CG, CHG, and CHH. Analyses were performed in biological triplicates for each variant. C Number of DMRs with higher methylation levels in F2000 (hypermethylated) and in F60 (hypomethylated). DMRs were investigated in the three DNA methylation contexts CG, CHG and CHH. Distribution of DMRs upstream in the putative promoter (4 kb of TSS), within the gene body, and down-stream in the putative terminator (4 kb of TTS) were analyzed in DMR-associated genes (q-value ≤ 0.01, methylation difference >|10%|). D Venn analysis of DMR-associated genes split in hyper- and hypomethylated promoters, gene bodies, and terminators. DMR, differentially methylated region; TSS, transcription start site; TTS, transcription termination site
Low Input Whole Genome Bisulfite Sequencing Prepared Dna, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/low input whole genome bisulfite sequencing prepared dna/product/Novogene
Average 86 stars, based on 1 article reviews
low input whole genome bisulfite sequencing prepared dna - by Bioz Stars, 2026-05
86/100 stars
  Buy from Supplier

86
Azenta genome bisulfite sequencing
<t>Whole-genome</t> <t>DNA</t> methylation analysis of Chinese yam variant F2000 and F60. A Principal component 1 and principal component 2 analyses were performed for each sample. B Methylation level distribution across genetic features including 4 kb upstream of TSS, gene body, and 4 kb downstream of TTS in the three DNA methylation contexts CG, CHG, and CHH. Analyses were performed in biological triplicates for each variant. C Number of DMRs with higher methylation levels in F2000 (hypermethylated) and in F60 (hypomethylated). DMRs were investigated in the three DNA methylation contexts CG, CHG and CHH. Distribution of DMRs upstream in the putative promoter (4 kb of TSS), within the gene body, and down-stream in the putative terminator (4 kb of TTS) were analyzed in DMR-associated genes (q-value ≤ 0.01, methylation difference >|10%|). D Venn analysis of DMR-associated genes split in hyper- and hypomethylated promoters, gene bodies, and terminators. DMR, differentially methylated region; TSS, transcription start site; TTS, transcription termination site
Genome Bisulfite Sequencing, supplied by Azenta, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/genome bisulfite sequencing/product/Azenta
Average 86 stars, based on 1 article reviews
genome bisulfite sequencing - by Bioz Stars, 2026-05
86/100 stars
  Buy from Supplier

99
Zymo Research bisulfite sequencing pcr bsp 458 ez dna methylation gold kit
<t>Whole-genome</t> <t>DNA</t> methylation analysis of Chinese yam variant F2000 and F60. A Principal component 1 and principal component 2 analyses were performed for each sample. B Methylation level distribution across genetic features including 4 kb upstream of TSS, gene body, and 4 kb downstream of TTS in the three DNA methylation contexts CG, CHG, and CHH. Analyses were performed in biological triplicates for each variant. C Number of DMRs with higher methylation levels in F2000 (hypermethylated) and in F60 (hypomethylated). DMRs were investigated in the three DNA methylation contexts CG, CHG and CHH. Distribution of DMRs upstream in the putative promoter (4 kb of TSS), within the gene body, and down-stream in the putative terminator (4 kb of TTS) were analyzed in DMR-associated genes (q-value ≤ 0.01, methylation difference >|10%|). D Venn analysis of DMR-associated genes split in hyper- and hypomethylated promoters, gene bodies, and terminators. DMR, differentially methylated region; TSS, transcription start site; TTS, transcription termination site
Bisulfite Sequencing Pcr Bsp 458 Ez Dna Methylation Gold Kit, supplied by Zymo Research, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/bisulfite sequencing pcr bsp 458 ez dna methylation gold kit/product/Zymo Research
Average 99 stars, based on 1 article reviews
bisulfite sequencing pcr bsp 458 ez dna methylation gold kit - by Bioz Stars, 2026-05
99/100 stars
  Buy from Supplier

95
Zymo Research representation bisulfite sequencing rrbs library preparation
<t>Whole-genome</t> <t>DNA</t> methylation analysis of Chinese yam variant F2000 and F60. A Principal component 1 and principal component 2 analyses were performed for each sample. B Methylation level distribution across genetic features including 4 kb upstream of TSS, gene body, and 4 kb downstream of TTS in the three DNA methylation contexts CG, CHG, and CHH. Analyses were performed in biological triplicates for each variant. C Number of DMRs with higher methylation levels in F2000 (hypermethylated) and in F60 (hypomethylated). DMRs were investigated in the three DNA methylation contexts CG, CHG and CHH. Distribution of DMRs upstream in the putative promoter (4 kb of TSS), within the gene body, and down-stream in the putative terminator (4 kb of TTS) were analyzed in DMR-associated genes (q-value ≤ 0.01, methylation difference >|10%|). D Venn analysis of DMR-associated genes split in hyper- and hypomethylated promoters, gene bodies, and terminators. DMR, differentially methylated region; TSS, transcription start site; TTS, transcription termination site
Representation Bisulfite Sequencing Rrbs Library Preparation, supplied by Zymo Research, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/representation bisulfite sequencing rrbs library preparation/product/Zymo Research
Average 95 stars, based on 1 article reviews
representation bisulfite sequencing rrbs library preparation - by Bioz Stars, 2026-05
95/100 stars
  Buy from Supplier

86
Gene Co Ltd bisulfite sequencing tbs method target gene bisulfite sequencing
<t>Whole-genome</t> <t>DNA</t> methylation analysis of Chinese yam variant F2000 and F60. A Principal component 1 and principal component 2 analyses were performed for each sample. B Methylation level distribution across genetic features including 4 kb upstream of TSS, gene body, and 4 kb downstream of TTS in the three DNA methylation contexts CG, CHG, and CHH. Analyses were performed in biological triplicates for each variant. C Number of DMRs with higher methylation levels in F2000 (hypermethylated) and in F60 (hypomethylated). DMRs were investigated in the three DNA methylation contexts CG, CHG and CHH. Distribution of DMRs upstream in the putative promoter (4 kb of TSS), within the gene body, and down-stream in the putative terminator (4 kb of TTS) were analyzed in DMR-associated genes (q-value ≤ 0.01, methylation difference >|10%|). D Venn analysis of DMR-associated genes split in hyper- and hypomethylated promoters, gene bodies, and terminators. DMR, differentially methylated region; TSS, transcription start site; TTS, transcription termination site
Bisulfite Sequencing Tbs Method Target Gene Bisulfite Sequencing, supplied by Gene Co Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/bisulfite sequencing tbs method target gene bisulfite sequencing/product/Gene Co Ltd
Average 86 stars, based on 1 article reviews
bisulfite sequencing tbs method target gene bisulfite sequencing - by Bioz Stars, 2026-05
86/100 stars
  Buy from Supplier

Image Search Results


Samples taken from the two MA pedigrees for different experiments. A) Ten MA lines were sampled from the two pedigrees. Samples for sequencing were taken after 5, 20, and 40 transfers and DNA methylation was detected using bisulfite sequencing (red circles). B) Three additional MA lines were sampled from both pedigrees and samples were taken after 1, 5, 7, 8, 10, and 15 transfers for Nanopore sequencing and after 5, 8, 10, 20, and 40 transfers for H3K9me3 ChIP-seq.

Journal: bioRxiv

Article Title: Centromeres are hotspots of cytosine methylation epimutations in a filamentous fungus

doi: 10.64898/2026.03.03.709258

Figure Lengend Snippet: Samples taken from the two MA pedigrees for different experiments. A) Ten MA lines were sampled from the two pedigrees. Samples for sequencing were taken after 5, 20, and 40 transfers and DNA methylation was detected using bisulfite sequencing (red circles). B) Three additional MA lines were sampled from both pedigrees and samples were taken after 1, 5, 7, 8, 10, and 15 transfers for Nanopore sequencing and after 5, 8, 10, 20, and 40 transfers for H3K9me3 ChIP-seq.

Article Snippet: For whole genome bisulfite sequencing, DNA samples were sent to Novogene (Cambridge, UK).

Techniques: Sequencing, DNA Methylation Assay, Methylation Sequencing, Nanopore Sequencing, ChIP-sequencing

Pairwise divergence in cytosine methylation patterns among the MA lines and their ancestors. X-axis shows the number of mitoses separating the two lines that are being compared, and the y-axis shows cytosine methylation divergence. Red line shows a neutral epimutation accumulation model fitted to all data, orange line shows a neutral epimutation accumulation model fitted to data with outlier samples removed, and solid blue line shows a logistic model fitted to all data, and the dotted line shows null model of no increase in divergence. A) The divergence calculated from single cytosines, for CG, CHG, and CHH sequence motifs. B) The divergence calculated for DMRs in different sequence contexts, as in panel A.

Journal: bioRxiv

Article Title: Centromeres are hotspots of cytosine methylation epimutations in a filamentous fungus

doi: 10.64898/2026.03.03.709258

Figure Lengend Snippet: Pairwise divergence in cytosine methylation patterns among the MA lines and their ancestors. X-axis shows the number of mitoses separating the two lines that are being compared, and the y-axis shows cytosine methylation divergence. Red line shows a neutral epimutation accumulation model fitted to all data, orange line shows a neutral epimutation accumulation model fitted to data with outlier samples removed, and solid blue line shows a logistic model fitted to all data, and the dotted line shows null model of no increase in divergence. A) The divergence calculated from single cytosines, for CG, CHG, and CHH sequence motifs. B) The divergence calculated for DMRs in different sequence contexts, as in panel A.

Article Snippet: For whole genome bisulfite sequencing, DNA samples were sent to Novogene (Cambridge, UK).

Techniques: Methylation, Sequencing

Whole-genome DNA methylation analysis of Chinese yam variant F2000 and F60. A Principal component 1 and principal component 2 analyses were performed for each sample. B Methylation level distribution across genetic features including 4 kb upstream of TSS, gene body, and 4 kb downstream of TTS in the three DNA methylation contexts CG, CHG, and CHH. Analyses were performed in biological triplicates for each variant. C Number of DMRs with higher methylation levels in F2000 (hypermethylated) and in F60 (hypomethylated). DMRs were investigated in the three DNA methylation contexts CG, CHG and CHH. Distribution of DMRs upstream in the putative promoter (4 kb of TSS), within the gene body, and down-stream in the putative terminator (4 kb of TTS) were analyzed in DMR-associated genes (q-value ≤ 0.01, methylation difference >|10%|). D Venn analysis of DMR-associated genes split in hyper- and hypomethylated promoters, gene bodies, and terminators. DMR, differentially methylated region; TSS, transcription start site; TTS, transcription termination site

Journal: BMC Plant Biology

Article Title: Insights into epigenetics suggest a role of DNA methylation in regulating Chinese yam tuber shape

doi: 10.1186/s12870-026-08438-5

Figure Lengend Snippet: Whole-genome DNA methylation analysis of Chinese yam variant F2000 and F60. A Principal component 1 and principal component 2 analyses were performed for each sample. B Methylation level distribution across genetic features including 4 kb upstream of TSS, gene body, and 4 kb downstream of TTS in the three DNA methylation contexts CG, CHG, and CHH. Analyses were performed in biological triplicates for each variant. C Number of DMRs with higher methylation levels in F2000 (hypermethylated) and in F60 (hypomethylated). DMRs were investigated in the three DNA methylation contexts CG, CHG and CHH. Distribution of DMRs upstream in the putative promoter (4 kb of TSS), within the gene body, and down-stream in the putative terminator (4 kb of TTS) were analyzed in DMR-associated genes (q-value ≤ 0.01, methylation difference >|10%|). D Venn analysis of DMR-associated genes split in hyper- and hypomethylated promoters, gene bodies, and terminators. DMR, differentially methylated region; TSS, transcription start site; TTS, transcription termination site

Article Snippet: Prepared DNA samples were sent to Novogene Company (Beijing, China) for low-input whole-genome bisulfite sequencing including the steps of bisulfite treatment and library construction.

Techniques: DNA Methylation Assay, Variant Assay, Methylation