paired end short read sequencing libraries Search Results


nonbreaking paired-end sequencing libraries  (BGI Shenzhen)
90
BGI Shenzhen nonbreaking paired-end sequencing libraries
Nonbreaking Paired End Sequencing Libraries, 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
https://www.bioz.com/product/paired+end+short+read+sequencing+libraries/nonbreaking+paired+end+sequencing+libraries/pmc08016264-357-6-6
Average 90 stars, based on 1 article reviews
nonbreaking paired-end sequencing libraries - by Bioz Stars, 2026-10
90/100 stars
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dnbseq™ short-read 150bp paired-end sequencing  (MGI Tech Co Ltd)
90
MGI Tech Co Ltd dnbseq™ short-read 150bp paired-end sequencing
Dnbseq™ Short Read 150bp Paired End 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
https://www.bioz.com/product/paired+end+short+read+sequencing+libraries/dnbseq++short+read+150bp+paired+end+sequencing/bio_rxiv__2024__04__29__591545-29-23-13
Average 90 stars, based on 1 article reviews
dnbseq™ short-read 150bp paired-end sequencing - by Bioz Stars, 2026-10
90/100 stars
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pcr-free library preparation and paired-end sequencing 2 × novaseq 525m  (Fasteris Life)
90
Fasteris Life pcr-free library preparation and paired-end sequencing 2 × novaseq 525m
Pcr Free Library Preparation And Paired End Sequencing 2 × Novaseq 525m, supplied by Fasteris Life, 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/product/paired+end+short+read+sequencing+libraries/pcr+free+library+preparation+and+paired+end+sequencing+2+%C3%97+novaseq+525m/bio_rxiv__2024__02__29__582456-144-4-15
Average 90 stars, based on 1 article reviews
pcr-free library preparation and paired-end sequencing 2 × novaseq 525m - by Bioz Stars, 2026-10
90/100 stars
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sequencing libraries 400-bp paired-end  (BGI Shenzhen)
90
BGI Shenzhen sequencing libraries 400-bp paired-end
(A) The log 2 fold-change values from whole genome <t>re-sequencing</t> data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).
Sequencing Libraries 400 Bp Paired End, 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
https://www.bioz.com/product/paired+end+short+read+sequencing+libraries/sequencing+libraries+400+bp+paired+end/pmc04890787-260-0-23
Average 90 stars, based on 1 article reviews
sequencing libraries 400-bp paired-end - by Bioz Stars, 2026-10
90/100 stars
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library for paired-end sequencing of 125 nt  (GATC Biotech)
90
GATC Biotech library for paired-end sequencing of 125 nt
(A) The log 2 fold-change values from whole genome <t>re-sequencing</t> data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).
Library For Paired End Sequencing Of 125 Nt, supplied by GATC 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/product/paired+end+short+read+sequencing+libraries/library+for+paired+end+sequencing+of+125+nt/pmc04979143-150-8-40
Average 90 stars, based on 1 article reviews
library for paired-end sequencing of 125 nt - by Bioz Stars, 2026-10
90/100 stars
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amplicon library preparation and paired-end sequencing (2)  (Fasteris Life)
90
Fasteris Life amplicon library preparation and paired-end sequencing (2)
(A) The log 2 fold-change values from whole genome <t>re-sequencing</t> data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).
Amplicon Library Preparation And Paired End Sequencing (2), supplied by Fasteris Life, 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/product/paired+end+short+read+sequencing+libraries/amplicon+library+preparation+and+paired+end+sequencing++2+/pmc08007739-362-17-6
Average 90 stars, based on 1 article reviews
amplicon library preparation and paired-end sequencing (2) - by Bioz Stars, 2026-10
90/100 stars
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300-bp paired-end sequencing libraries nextera tag-mentation sequencing kits  (Nextera AS)
90
Nextera AS 300-bp paired-end sequencing libraries nextera tag-mentation sequencing kits
(A) The log 2 fold-change values from whole genome <t>re-sequencing</t> data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).
300 Bp Paired End Sequencing Libraries Nextera Tag Mentation Sequencing Kits, supplied by Nextera AS, 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/product/paired+end+short+read+sequencing+libraries/300+bp+paired+end+sequencing+libraries+nextera+tag+mentation+sequencing+kits/pmc05955891-252-9-13
Average 90 stars, based on 1 article reviews
300-bp paired-end sequencing libraries nextera tag-mentation sequencing kits - by Bioz Stars, 2026-10
90/100 stars
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human sequence na12878  (Broad Institute Inc)
90
Broad Institute Inc human sequence na12878
(A) The log 2 fold-change values from whole genome <t>re-sequencing</t> data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).
Human Sequence Na12878, 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/product/paired+end+short+read+sequencing+libraries/paired+end+libraries+from+the+human+sequence+na12878/pmc03198573-321-12-19
Average 90 stars, based on 1 article reviews
human sequence na12878 - by Bioz Stars, 2026-10
90/100 stars
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dual-sequencing approach (54-mer single read (se) and 108-mer pair-end read (pe)  (Fasteris Life)
90
Fasteris Life dual-sequencing approach (54-mer single read (se) and 108-mer pair-end read (pe)
(A) The log 2 fold-change values from whole genome <t>re-sequencing</t> data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).
Dual Sequencing Approach (54 Mer Single Read (Se) And 108 Mer Pair End Read (Pe), supplied by Fasteris Life, 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/product/paired+end+short+read+sequencing+libraries/dual+sequencing+approach++54+mer+single+read++se++and+108+mer+pair+end+read++pe+/pmc07397075-76-18-10
Average 90 stars, based on 1 article reviews
dual-sequencing approach (54-mer single read (se) and 108-mer pair-end read (pe) - by Bioz Stars, 2026-10
90/100 stars
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paired-end read sequencing  (LGC Genomics GmbH)
90
LGC Genomics GmbH paired-end read sequencing
(A) The log 2 fold-change values from whole genome <t>re-sequencing</t> data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).
Paired End Read Sequencing, supplied by LGC Genomics GmbH, 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/product/paired+end+short+read+sequencing+libraries/paired+end+read+sequencing/10__3389_slash_fmars__2020__00266-121-23-29
Average 90 stars, based on 1 article reviews
paired-end read sequencing - by Bioz Stars, 2026-10
90/100 stars
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base calling, demultiplexing, adapter and primer sequence clipping, paired-end read merging  (LGC Genomics GmbH)
90
LGC Genomics GmbH base calling, demultiplexing, adapter and primer sequence clipping, paired-end read merging
(A) The log 2 fold-change values from whole genome <t>re-sequencing</t> data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).
Base Calling, Demultiplexing, Adapter And Primer Sequence Clipping, Paired End Read Merging, supplied by LGC Genomics GmbH, 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/product/paired+end+short+read+sequencing+libraries/base+calling++demultiplexing++adapter+and+primer+sequence+clipping++paired+end+read+merging/pm39128858-87-8-13
Average 90 stars, based on 1 article reviews
base calling, demultiplexing, adapter and primer sequence clipping, paired-end read merging - by Bioz Stars, 2026-10
90/100 stars
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150-bp paired-end sequencing library  (MGI Tech Co Ltd)
90
MGI Tech Co Ltd 150-bp paired-end sequencing library
(A) The log 2 fold-change values from whole genome <t>re-sequencing</t> data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).
150 Bp Paired End Sequencing Library, 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
https://www.bioz.com/product/paired+end+short+read+sequencing+libraries/150+bp+paired+end+sequencing+library/pm39290157-35-6-17
Average 90 stars, based on 1 article reviews
150-bp paired-end sequencing library - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

Image Search Results


(A) The log 2 fold-change values from whole genome re-sequencing data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).

Journal: PLoS Genetics

Article Title: A Complex Structural Variation on Chromosome 27 Leads to the Ectopic Expression of HOXB8 and the Muffs and Beard Phenotype in Chickens

doi: 10.1371/journal.pgen.1006071

Figure Lengend Snippet: (A) The log 2 fold-change values from whole genome re-sequencing data illustrating the read depth differences between the HB and HQLA breeds. This analysis validates the presence of the CNVs on GGA27 in chickens with the Muffs and beard phenotype that were previously identified using a CGH array experiment. (B) Schematic illustration of the CNV rearrangements in the Mb locus on GGA27. (C) Genes located within the three duplicated CNV regions include the 3’ sequence of PSMC5 and entire SMARCD2 in CNV1 (green shadow), entire HOXB8 and HOXB7 in CNV2 (blue shadow), 5’ sequence of CCR7 , 3’ sequence of KRT222 , and entire SMARCE1 in CNV3 (pink shadow).

Article Snippet: Sequencing libraries (170-bp paired-end, 400-bp paired-end and 3-kb mate-pair) were constructed, and whole-genome re-sequencing was performed using the Illumina HiSeq 2000 platform by BGI (Shenzhen).

Techniques: Sequencing

The duplicated regions identified by array-CGH are illustrated by green (CNV1), blue (CNV2) and pink (CNV3) boxes, respectively. (A) The boundaries of the CNVs were tested using 8 primers indicated by the arrows located in the known duplicated region of CNV1 and CNV3. All possible amplifications were considered and performed in both Mb and wild-type chickens. (B) The breakpoints of both CNV1_3’ (1,721,521 bp) and CNV3_5’ (4,470,331 bp) were identified after sequencing the specifically-amplified PCR product obtained in Mb chickens using primer F1 and R2. An overlap of two nucleotides was detected in the junction region. Outward facing primers (green and pink arrows) were designed to analyze the other boundary of CNV1 and CNV3. (C) CNV2 was found to be located next to CNV3 in chickens with the Mb phenotype using a genome-walking strategy. The breakpoints of both CNV3_3’ (4,503,417 bp) and CNV2_5’ (3,578,409 bp) were verified by sequencing. A two-nucleotide insertion was found in the junction region. (D) The breakpoints of both CNV2_3’ (3,592,890 bp) and CNV1_5’ (1,702,269 bp) were confirmed through unmapped read alignment of whole genome re-sequencing data. An eight-base insertion was detected in the junction.

Journal: PLoS Genetics

Article Title: A Complex Structural Variation on Chromosome 27 Leads to the Ectopic Expression of HOXB8 and the Muffs and Beard Phenotype in Chickens

doi: 10.1371/journal.pgen.1006071

Figure Lengend Snippet: The duplicated regions identified by array-CGH are illustrated by green (CNV1), blue (CNV2) and pink (CNV3) boxes, respectively. (A) The boundaries of the CNVs were tested using 8 primers indicated by the arrows located in the known duplicated region of CNV1 and CNV3. All possible amplifications were considered and performed in both Mb and wild-type chickens. (B) The breakpoints of both CNV1_3’ (1,721,521 bp) and CNV3_5’ (4,470,331 bp) were identified after sequencing the specifically-amplified PCR product obtained in Mb chickens using primer F1 and R2. An overlap of two nucleotides was detected in the junction region. Outward facing primers (green and pink arrows) were designed to analyze the other boundary of CNV1 and CNV3. (C) CNV2 was found to be located next to CNV3 in chickens with the Mb phenotype using a genome-walking strategy. The breakpoints of both CNV3_3’ (4,503,417 bp) and CNV2_5’ (3,578,409 bp) were verified by sequencing. A two-nucleotide insertion was found in the junction region. (D) The breakpoints of both CNV2_3’ (3,592,890 bp) and CNV1_5’ (1,702,269 bp) were confirmed through unmapped read alignment of whole genome re-sequencing data. An eight-base insertion was detected in the junction.

Article Snippet: Sequencing libraries (170-bp paired-end, 400-bp paired-end and 3-kb mate-pair) were constructed, and whole-genome re-sequencing was performed using the Illumina HiSeq 2000 platform by BGI (Shenzhen).

Techniques: Sequencing, Amplification