sequencing data quality control Search Results


high-quality sequence data  (Broad Institute Inc)
90
Broad Institute Inc high-quality sequence data
High Quality Sequence Data, 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
https://www.bioz.com/result/high-quality sequence data/product/Broad Institute Inc
Average 90 stars, based on 1 article reviews
high-quality sequence data - by Bioz Stars, 2026-03
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post-sequencing quality control  (Novogene)
90
Novogene post-sequencing quality control
Post Sequencing Quality Control, supplied by Novogene, 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/post-sequencing quality control/product/Novogene
Average 90 stars, based on 1 article reviews
post-sequencing quality control - by Bioz Stars, 2026-03
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oligo-probes based on 18 different phage lambda sequences and 63 different quality controls (qc)  (CombiMatrix)
90
CombiMatrix oligo-probes based on 18 different phage lambda sequences and 63 different quality controls (qc)
Oligo Probes Based On 18 Different Phage Lambda Sequences And 63 Different Quality Controls (Qc), supplied by CombiMatrix, 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/oligo-probes based on 18 different phage lambda sequences and 63 different quality controls (qc)/product/CombiMatrix
Average 90 stars, based on 1 article reviews
oligo-probes based on 18 different phage lambda sequences and 63 different quality controls (qc) - by Bioz Stars, 2026-03
90/100 stars
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quality-controlled sequences  (Illumina Inc)
90
Illumina Inc quality-controlled sequences
Quality Controlled Sequences, 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
https://www.bioz.com/result/quality-controlled sequences/product/Illumina Inc
Average 90 stars, based on 1 article reviews
quality-controlled sequences - by Bioz Stars, 2026-03
90/100 stars
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library construction, quality control, and sequencing  (Novogene)
90
Novogene library construction, quality control, and sequencing
Library Construction, Quality Control, And Sequencing, supplied by Novogene, 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/library construction, quality control, and sequencing/product/Novogene
Average 90 stars, based on 1 article reviews
library construction, quality control, and sequencing - by Bioz Stars, 2026-03
90/100 stars
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sequencing data quality control  (Sequentia Biotech)
90
Sequentia Biotech sequencing data quality control
General analysis in Trichoderma atroviride T11-treated (T11) Solanum lycopersicum or untreated (C) plants libraries. ( A ) Length distribution and abundance of the miRNAs that showed at least 10 read counts against their miRNA* <t>sequence</t> in S. lycopersicum plants treated (T11) or not (C). The percentage is calculated over the total number of reads that aligned to the miRNA candidates identified in plants from both conditions (including those with less than 10 read counts against their miRNA* sequence and/or those that were solely transcribed in one sample per condition). The length of the miRNAs identified ranged from 20–24 nt; ( B ) Venn diagram showing the number of miRNAs (that displayed at least 10 read counts against their miRNA* sequence) identified in both conditions, solely in T11 (green) or in untreated control plants (blue).
Sequencing Data Quality Control, supplied by Sequentia Biotech, 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/sequencing data quality control/product/Sequentia Biotech
Average 90 stars, based on 1 article reviews
sequencing data quality control - by Bioz Stars, 2026-03
90/100 stars
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rna isolation, preparation of rna library and transcriptome sequencing  (Novogene)
90
Novogene rna isolation, preparation of rna library and transcriptome sequencing
Knock-out analysis of hs654 and hs267/hs266/hs853 enhancers. a,b, Predicted chromatin interactions (black arches) between enhancers (green boxes) and target genes (black boxes) are shown. Gene and enhancer models are not drawn to scale. c,d, <t>Transcriptome-wide</t> mRNA expression changes in E11.5 whole midbrain (MB) of hs654 knock-out mice (c) and in E11.5 forebrain (FB) of hs267/hs266/hs853 knockout mice (d) relative to wildtype mice (WT). Points indicate individual genes, with blue indicating statistically significant differences after adjustment for multiple comparisons (Padj < 0.05). N. S., not significant. P values were calculated using DESeq2.
Rna Isolation, Preparation Of Rna Library And Transcriptome Sequencing, supplied by Novogene, 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/rna isolation, preparation of rna library and transcriptome sequencing/product/Novogene
Average 90 stars, based on 1 article reviews
rna isolation, preparation of rna library and transcriptome sequencing - by Bioz Stars, 2026-03
90/100 stars
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library quality control and sequencing  (Novogene)
90
Novogene library quality control and sequencing
Knock-out analysis of hs654 and hs267/hs266/hs853 enhancers. a,b, Predicted chromatin interactions (black arches) between enhancers (green boxes) and target genes (black boxes) are shown. Gene and enhancer models are not drawn to scale. c,d, <t>Transcriptome-wide</t> mRNA expression changes in E11.5 whole midbrain (MB) of hs654 knock-out mice (c) and in E11.5 forebrain (FB) of hs267/hs266/hs853 knockout mice (d) relative to wildtype mice (WT). Points indicate individual genes, with blue indicating statistically significant differences after adjustment for multiple comparisons (Padj < 0.05). N. S., not significant. P values were calculated using DESeq2.
Library Quality Control And Sequencing, supplied by Novogene, 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/library quality control and sequencing/product/Novogene
Average 90 stars, based on 1 article reviews
library quality control and sequencing - by Bioz Stars, 2026-03
90/100 stars
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sequencing data quality control  (Adaptive Biotechnologies Corp)
90
Adaptive Biotechnologies Corp sequencing data quality control
Bulk TCRβ <t>sequencing</t> from BMC and PBMC individuals who had paired samples available and at least 1,000 TCRβ templates in the BMC sample (n=11). The frequencies of TCRβ clonotypes in the two compartments were compared using the immunoSEQ® Differential Abundance Tool. TCRβ repertoire overlap was analyzed using the Morisita index (M.I., value inset). As a control, TCRβ clonotypes from an individual’s PBMCs obtained 9 days and 17 days after 2 nd mRNA vaccine dose were compared (upper left plot).
Sequencing Data Quality Control, supplied by Adaptive Biotechnologies Corp, 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/sequencing data quality control/product/Adaptive Biotechnologies Corp
Average 90 stars, based on 1 article reviews
sequencing data quality control - by Bioz Stars, 2026-03
90/100 stars
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10× sequencing read processing and quality control  (Novogene)
90
Novogene 10× sequencing read processing and quality control
Bulk TCRβ <t>sequencing</t> from BMC and PBMC individuals who had paired samples available and at least 1,000 TCRβ templates in the BMC sample (n=11). The frequencies of TCRβ clonotypes in the two compartments were compared using the immunoSEQ® Differential Abundance Tool. TCRβ repertoire overlap was analyzed using the Morisita index (M.I., value inset). As a control, TCRβ clonotypes from an individual’s PBMCs obtained 9 days and 17 days after 2 nd mRNA vaccine dose were compared (upper left plot).
10× Sequencing Read Processing And Quality Control, supplied by Novogene, 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/10× sequencing read processing and quality control/product/Novogene
Average 90 stars, based on 1 article reviews
10× sequencing read processing and quality control - by Bioz Stars, 2026-03
90/100 stars
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control region sequence data  (Rocha labs)
90
Rocha labs control region sequence data
Bulk TCRβ <t>sequencing</t> from BMC and PBMC individuals who had paired samples available and at least 1,000 TCRβ templates in the BMC sample (n=11). The frequencies of TCRβ clonotypes in the two compartments were compared using the immunoSEQ® Differential Abundance Tool. TCRβ repertoire overlap was analyzed using the Morisita index (M.I., value inset). As a control, TCRβ clonotypes from an individual’s PBMCs obtained 9 days and 17 days after 2 nd mRNA vaccine dose were compared (upper left plot).
Control Region Sequence Data, supplied by Rocha labs, 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/control region sequence data/product/Rocha labs
Average 90 stars, based on 1 article reviews
control region sequence data - by Bioz Stars, 2026-03
90/100 stars
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quality control and sequencing of construted libraries  (Novogene)
90
Novogene quality control and sequencing of construted libraries
Bulk TCRβ <t>sequencing</t> from BMC and PBMC individuals who had paired samples available and at least 1,000 TCRβ templates in the BMC sample (n=11). The frequencies of TCRβ clonotypes in the two compartments were compared using the immunoSEQ® Differential Abundance Tool. TCRβ repertoire overlap was analyzed using the Morisita index (M.I., value inset). As a control, TCRβ clonotypes from an individual’s PBMCs obtained 9 days and 17 days after 2 nd mRNA vaccine dose were compared (upper left plot).
Quality Control And Sequencing Of Construted Libraries, supplied by Novogene, 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/quality control and sequencing of construted libraries/product/Novogene
Average 90 stars, based on 1 article reviews
quality control and sequencing of construted libraries - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

Image Search Results


General analysis in Trichoderma atroviride T11-treated (T11) Solanum lycopersicum or untreated (C) plants libraries. ( A ) Length distribution and abundance of the miRNAs that showed at least 10 read counts against their miRNA* sequence in S. lycopersicum plants treated (T11) or not (C). The percentage is calculated over the total number of reads that aligned to the miRNA candidates identified in plants from both conditions (including those with less than 10 read counts against their miRNA* sequence and/or those that were solely transcribed in one sample per condition). The length of the miRNAs identified ranged from 20–24 nt; ( B ) Venn diagram showing the number of miRNAs (that displayed at least 10 read counts against their miRNA* sequence) identified in both conditions, solely in T11 (green) or in untreated control plants (blue).

Journal: International Journal of Molecular Sciences

Article Title: Identification of Tomato microRNAs in Late Response to Trichoderma atroviride

doi: 10.3390/ijms25031617

Figure Lengend Snippet: General analysis in Trichoderma atroviride T11-treated (T11) Solanum lycopersicum or untreated (C) plants libraries. ( A ) Length distribution and abundance of the miRNAs that showed at least 10 read counts against their miRNA* sequence in S. lycopersicum plants treated (T11) or not (C). The percentage is calculated over the total number of reads that aligned to the miRNA candidates identified in plants from both conditions (including those with less than 10 read counts against their miRNA* sequence and/or those that were solely transcribed in one sample per condition). The length of the miRNAs identified ranged from 20–24 nt; ( B ) Venn diagram showing the number of miRNAs (that displayed at least 10 read counts against their miRNA* sequence) identified in both conditions, solely in T11 (green) or in untreated control plants (blue).

Article Snippet: Quality control of the sequencing data and the identification of known and novel miRNA candidates were performed by Sequentia Biotech S.L. (Barcelona, Spain) as follows.

Techniques: Sequencing, Control

Knock-out analysis of hs654 and hs267/hs266/hs853 enhancers. a,b, Predicted chromatin interactions (black arches) between enhancers (green boxes) and target genes (black boxes) are shown. Gene and enhancer models are not drawn to scale. c,d, Transcriptome-wide mRNA expression changes in E11.5 whole midbrain (MB) of hs654 knock-out mice (c) and in E11.5 forebrain (FB) of hs267/hs266/hs853 knockout mice (d) relative to wildtype mice (WT). Points indicate individual genes, with blue indicating statistically significant differences after adjustment for multiple comparisons (Padj < 0.05). N. S., not significant. P values were calculated using DESeq2.

Journal: Nature genetics

Article Title: Increased Enhancer—Promoter Interactions during Developmental Enhancer Activation in Mammals

doi: 10.1038/s41588-024-01681-2

Figure Lengend Snippet: Knock-out analysis of hs654 and hs267/hs266/hs853 enhancers. a,b, Predicted chromatin interactions (black arches) between enhancers (green boxes) and target genes (black boxes) are shown. Gene and enhancer models are not drawn to scale. c,d, Transcriptome-wide mRNA expression changes in E11.5 whole midbrain (MB) of hs654 knock-out mice (c) and in E11.5 forebrain (FB) of hs267/hs266/hs853 knockout mice (d) relative to wildtype mice (WT). Points indicate individual genes, with blue indicating statistically significant differences after adjustment for multiple comparisons (Padj < 0.05). N. S., not significant. P values were calculated using DESeq2.

Article Snippet: RNA isolation, preparation of RNA library and transcriptome sequencing was conducted by Novogene Co., LTD (Beijing, China).

Techniques: Knock-Out, Expressing

Bulk TCRβ sequencing from BMC and PBMC individuals who had paired samples available and at least 1,000 TCRβ templates in the BMC sample (n=11). The frequencies of TCRβ clonotypes in the two compartments were compared using the immunoSEQ® Differential Abundance Tool. TCRβ repertoire overlap was analyzed using the Morisita index (M.I., value inset). As a control, TCRβ clonotypes from an individual’s PBMCs obtained 9 days and 17 days after 2 nd mRNA vaccine dose were compared (upper left plot).

Journal: medRxiv

Article Title: Spike-specific T cells are enriched in breastmilk following SARS-CoV-2 mRNA vaccination

doi: 10.1101/2021.12.03.21267036

Figure Lengend Snippet: Bulk TCRβ sequencing from BMC and PBMC individuals who had paired samples available and at least 1,000 TCRβ templates in the BMC sample (n=11). The frequencies of TCRβ clonotypes in the two compartments were compared using the immunoSEQ® Differential Abundance Tool. TCRβ repertoire overlap was analyzed using the Morisita index (M.I., value inset). As a control, TCRβ clonotypes from an individual’s PBMCs obtained 9 days and 17 days after 2 nd mRNA vaccine dose were compared (upper left plot).

Article Snippet: Quality control of sequencing data was performed by Adaptive Biotechnologies.

Techniques: Sequencing, Control