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90
CLC Bio clc genomics workbench v10.1
Clc Genomics Workbench V10.1, supplied by CLC Bio, 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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AUTODOCK GmbH gnina v1.0.1 software
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Esri inc software arcgis v10.1
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Thermo Fisher sds® v1.0.1 software supplied with the instrument
Sds® V1.0.1 Software Supplied With The Instrument, supplied by Thermo Fisher, 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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Agilent technologies feature extraction v10.1.1
Feature Extraction V10.1.1, supplied by Agilent 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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GENETYX CORPORATION genetyx-mac v10.1
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Agilent technologies feature extraction software v10.1.1.1
Feature Extraction Software V10.1.1.1, supplied by Agilent 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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Thermo Fisher chromosome analysis suite (chas) v1.0.1/na30.1
Chromosome Analysis Suite (Chas) V1.0.1/Na30.1, supplied by Thermo Fisher, 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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Becton Dickinson fcap array v1.0.1 software
Fcap Array V1.0.1 Software, supplied by Becton Dickinson, 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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Evident Corporation broadband sensor type v101-rb
Parameters of the AE sensors used to determine the frequency of acoustic signals emitted by PD in oil–paper insulation.
Broadband Sensor Type V101 Rb, supplied by Evident Corporation, 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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Agilent technologies v10.1 oligo
Triplication followed by ROH shows DUP-TRP/INV-DUP pattern. a Agilent aCGH <t>(V10.1)</t> plot of chromosome 14q23.2q23.3 region harboring a 2.2-Mb triplication (TRP; log2 ratio 1). b Agilent tiling high-density aCGH revealed a triplication (TRP; blue box) flanked by small duplications (DUP; red boxes) at both centromeric (Jct2) and telomeric junctions (Jct1) ( c ). d Color-matched sequence alignment of Jct1 and Jct2. Sequencing data of long-range PCR product was obtained by standard Sanger. Structure is now defined as DUP-TRP/INV-DUP. Genomic reference segments are displayed in blue (PROX, proximal) and red (DIST, distal). Strand orientation is indicated in parentheses. Microhomology at the junction is represented in black. e Read depth coverage plot of 17.7 Mb segment of 14q (chr14: 54,179,300-71,874,900) that includes the DUP-TRP/INV-DUP region. Normalized read depth coverage confirms the relative copy-number differences along the CGR consistent with a triplication (31.8/15.8 = 2) flanked by duplications (DUP1 = 20.1/15.8 = 1.3; DUP2 = 18.3/15.8 = 1.2). Y -axis: read depth coverage; X -axis: 100 bp bins at 14q. Genomic coordinates are in hg19
V10.1 Oligo, supplied by Agilent 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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GraphPad Software Inc prism v10.1.1 software
Triplication followed by ROH shows DUP-TRP/INV-DUP pattern. a Agilent aCGH <t>(V10.1)</t> plot of chromosome 14q23.2q23.3 region harboring a 2.2-Mb triplication (TRP; log2 ratio 1). b Agilent tiling high-density aCGH revealed a triplication (TRP; blue box) flanked by small duplications (DUP; red boxes) at both centromeric (Jct2) and telomeric junctions (Jct1) ( c ). d Color-matched sequence alignment of Jct1 and Jct2. Sequencing data of long-range PCR product was obtained by standard Sanger. Structure is now defined as DUP-TRP/INV-DUP. Genomic reference segments are displayed in blue (PROX, proximal) and red (DIST, distal). Strand orientation is indicated in parentheses. Microhomology at the junction is represented in black. e Read depth coverage plot of 17.7 Mb segment of 14q (chr14: 54,179,300-71,874,900) that includes the DUP-TRP/INV-DUP region. Normalized read depth coverage confirms the relative copy-number differences along the CGR consistent with a triplication (31.8/15.8 = 2) flanked by duplications (DUP1 = 20.1/15.8 = 1.3; DUP2 = 18.3/15.8 = 1.2). Y -axis: read depth coverage; X -axis: 100 bp bins at 14q. Genomic coordinates are in hg19
Prism V10.1.1 Software, supplied by GraphPad Software 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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Image Search Results


Parameters of the AE sensors used to determine the frequency of acoustic signals emitted by PD in oil–paper insulation.

Journal: Sensors (Basel, Switzerland)

Article Title: Development of Acoustic Emission Sensor Optimized for Partial Discharge Monitoring in Power Transformers

doi: 10.3390/s19081865

Figure Lengend Snippet: Parameters of the AE sensors used to determine the frequency of acoustic signals emitted by PD in oil–paper insulation.

Article Snippet: The frequency analysis of the AE pulses registered with prototype sensor A6890 ( ) showed large similarity to the results obtained with broadband sensor type Olympus V101-RB.

Techniques:

Average normalized power spectrum density (PSD) determined for acoustic emission (AE) signals emitted by surface discharges (generated in electrode system A) and registered with the use of ultrasonic sensor type: ( a ) Olympus V101-RB, ( b ) PAC WD, ( c ) PAC R15D, and ( d ) PAC D9241A.

Journal: Sensors (Basel, Switzerland)

Article Title: Development of Acoustic Emission Sensor Optimized for Partial Discharge Monitoring in Power Transformers

doi: 10.3390/s19081865

Figure Lengend Snippet: Average normalized power spectrum density (PSD) determined for acoustic emission (AE) signals emitted by surface discharges (generated in electrode system A) and registered with the use of ultrasonic sensor type: ( a ) Olympus V101-RB, ( b ) PAC WD, ( c ) PAC R15D, and ( d ) PAC D9241A.

Article Snippet: The frequency analysis of the AE pulses registered with prototype sensor A6890 ( ) showed large similarity to the results obtained with broadband sensor type Olympus V101-RB.

Techniques: Generated

Average normalized PSD determined for AE signals emitted by surface discharges (generated in the electrode system B) and registered with the use of ultrasonic sensor type: ( a ) Olympus V101-RB, ( b ) PAC WD, ( c ) PAC R15D, and ( d ) PAC D9241A.

Journal: Sensors (Basel, Switzerland)

Article Title: Development of Acoustic Emission Sensor Optimized for Partial Discharge Monitoring in Power Transformers

doi: 10.3390/s19081865

Figure Lengend Snippet: Average normalized PSD determined for AE signals emitted by surface discharges (generated in the electrode system B) and registered with the use of ultrasonic sensor type: ( a ) Olympus V101-RB, ( b ) PAC WD, ( c ) PAC R15D, and ( d ) PAC D9241A.

Article Snippet: The frequency analysis of the AE pulses registered with prototype sensor A6890 ( ) showed large similarity to the results obtained with broadband sensor type Olympus V101-RB.

Techniques: Generated

Average normalized PSD determined for AE signals emitted by interturn discharges and registered with the use of ultrasonic sensor type: ( a ) Olympus V101-RB, ( b ) PAC WD, ( c ) PAC R15D, and ( d ) PAC D9241A.

Journal: Sensors (Basel, Switzerland)

Article Title: Development of Acoustic Emission Sensor Optimized for Partial Discharge Monitoring in Power Transformers

doi: 10.3390/s19081865

Figure Lengend Snippet: Average normalized PSD determined for AE signals emitted by interturn discharges and registered with the use of ultrasonic sensor type: ( a ) Olympus V101-RB, ( b ) PAC WD, ( c ) PAC R15D, and ( d ) PAC D9241A.

Article Snippet: The frequency analysis of the AE pulses registered with prototype sensor A6890 ( ) showed large similarity to the results obtained with broadband sensor type Olympus V101-RB.

Techniques:

Average normalized PSD determined for AE signals emitted by partial discharges in oil and registered with the use of ultrasonic sensor type: ( a ) Olympus V101-RB, ( b ) PAC WD, ( c ) PAC R15D, and ( d ) PAC D9241A.

Journal: Sensors (Basel, Switzerland)

Article Title: Development of Acoustic Emission Sensor Optimized for Partial Discharge Monitoring in Power Transformers

doi: 10.3390/s19081865

Figure Lengend Snippet: Average normalized PSD determined for AE signals emitted by partial discharges in oil and registered with the use of ultrasonic sensor type: ( a ) Olympus V101-RB, ( b ) PAC WD, ( c ) PAC R15D, and ( d ) PAC D9241A.

Article Snippet: The frequency analysis of the AE pulses registered with prototype sensor A6890 ( ) showed large similarity to the results obtained with broadband sensor type Olympus V101-RB.

Techniques:

Frequency-domain parameters determined on the basis of the average PSD of AE pulses emitted by the investigated forms of partial discharges.

Journal: Sensors (Basel, Switzerland)

Article Title: Development of Acoustic Emission Sensor Optimized for Partial Discharge Monitoring in Power Transformers

doi: 10.3390/s19081865

Figure Lengend Snippet: Frequency-domain parameters determined on the basis of the average PSD of AE pulses emitted by the investigated forms of partial discharges.

Article Snippet: The frequency analysis of the AE pulses registered with prototype sensor A6890 ( ) showed large similarity to the results obtained with broadband sensor type Olympus V101-RB.

Techniques:

Triplication followed by ROH shows DUP-TRP/INV-DUP pattern. a Agilent aCGH (V10.1) plot of chromosome 14q23.2q23.3 region harboring a 2.2-Mb triplication (TRP; log2 ratio 1). b Agilent tiling high-density aCGH revealed a triplication (TRP; blue box) flanked by small duplications (DUP; red boxes) at both centromeric (Jct2) and telomeric junctions (Jct1) ( c ). d Color-matched sequence alignment of Jct1 and Jct2. Sequencing data of long-range PCR product was obtained by standard Sanger. Structure is now defined as DUP-TRP/INV-DUP. Genomic reference segments are displayed in blue (PROX, proximal) and red (DIST, distal). Strand orientation is indicated in parentheses. Microhomology at the junction is represented in black. e Read depth coverage plot of 17.7 Mb segment of 14q (chr14: 54,179,300-71,874,900) that includes the DUP-TRP/INV-DUP region. Normalized read depth coverage confirms the relative copy-number differences along the CGR consistent with a triplication (31.8/15.8 = 2) flanked by duplications (DUP1 = 20.1/15.8 = 1.3; DUP2 = 18.3/15.8 = 1.2). Y -axis: read depth coverage; X -axis: 100 bp bins at 14q. Genomic coordinates are in hg19

Journal: Genome Medicine

Article Title: Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome

doi: 10.1186/s13073-019-0633-y

Figure Lengend Snippet: Triplication followed by ROH shows DUP-TRP/INV-DUP pattern. a Agilent aCGH (V10.1) plot of chromosome 14q23.2q23.3 region harboring a 2.2-Mb triplication (TRP; log2 ratio 1). b Agilent tiling high-density aCGH revealed a triplication (TRP; blue box) flanked by small duplications (DUP; red boxes) at both centromeric (Jct2) and telomeric junctions (Jct1) ( c ). d Color-matched sequence alignment of Jct1 and Jct2. Sequencing data of long-range PCR product was obtained by standard Sanger. Structure is now defined as DUP-TRP/INV-DUP. Genomic reference segments are displayed in blue (PROX, proximal) and red (DIST, distal). Strand orientation is indicated in parentheses. Microhomology at the junction is represented in black. e Read depth coverage plot of 17.7 Mb segment of 14q (chr14: 54,179,300-71,874,900) that includes the DUP-TRP/INV-DUP region. Normalized read depth coverage confirms the relative copy-number differences along the CGR consistent with a triplication (31.8/15.8 = 2) flanked by duplications (DUP1 = 20.1/15.8 = 1.3; DUP2 = 18.3/15.8 = 1.2). Y -axis: read depth coverage; X -axis: 100 bp bins at 14q. Genomic coordinates are in hg19

Article Snippet: Structural variation and AOH in subject BAB7004 were identified by clinical chromosome microarray analysis (CMA) using V10.1 OLIGO [ ] which is a custom-designed array with approximately 400,000 interrogating oligonucleotides that include 60,000 probes used for assaying single-nucleotide polymorphisms (SNPs) (Agilent Technologies, Inc., Santa Clara, CA, USA) [ ].

Techniques: Sequencing

SNP analysis enabled AOH/ROH detection in addition to a copy-number neutral junction supporting underlying replication-based mechanism. a Agilent aCGH (V10.1) SNP array data (B-allele frequency, BAF) for chromosome 14 indicates a 42.2 Mb of AOH. b Top: pedigree structure of family HOU2583; Bottom: Illumina SNP array HumanOmniExpress-24 Beadchip B-allele frequency (BAF) plot of ~ 42 Mb telomeric segment spanning 14q (chr14:62584057-107287663) reveals a de novo complex genomic rearrangement (CGR) and ROH/AOH exclusively present in BAB7004 (please refer to Additional file : Figure S1 for SNP array results in other family members). BAF revealed that the TRP segment presents two distinct genotypes: a small one (92 kb) with unequal allele dosage, followed by a larger one with equal allele dosage (2.2 Mb). Unequal allele dosage TRP, light blue rectangle; equal allele dosage TRP, dark blue rectangle; flanking small DUP, red rectangle; AOH, orange rectangle. c Expected BAF genotypes for distinct copy-number states. d Color-matched schematic model of the 14q23.2q23.3 CGR formation in BAB7004. CGR presents at least three breakpoint junctions, i.e. Jct1, Jct2, Jct3, which are hypothesized to be generated by template switches during replication-based repair (see main text for discussion). Top: genomic coordinates of junctions inferred from multiple technical approaches. Bottom: representation of the SNP allele dosage in each segment involved in this CGR. A, B: SNP alleles. Genomic coordinates are in hg19

Journal: Genome Medicine

Article Title: Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome

doi: 10.1186/s13073-019-0633-y

Figure Lengend Snippet: SNP analysis enabled AOH/ROH detection in addition to a copy-number neutral junction supporting underlying replication-based mechanism. a Agilent aCGH (V10.1) SNP array data (B-allele frequency, BAF) for chromosome 14 indicates a 42.2 Mb of AOH. b Top: pedigree structure of family HOU2583; Bottom: Illumina SNP array HumanOmniExpress-24 Beadchip B-allele frequency (BAF) plot of ~ 42 Mb telomeric segment spanning 14q (chr14:62584057-107287663) reveals a de novo complex genomic rearrangement (CGR) and ROH/AOH exclusively present in BAB7004 (please refer to Additional file : Figure S1 for SNP array results in other family members). BAF revealed that the TRP segment presents two distinct genotypes: a small one (92 kb) with unequal allele dosage, followed by a larger one with equal allele dosage (2.2 Mb). Unequal allele dosage TRP, light blue rectangle; equal allele dosage TRP, dark blue rectangle; flanking small DUP, red rectangle; AOH, orange rectangle. c Expected BAF genotypes for distinct copy-number states. d Color-matched schematic model of the 14q23.2q23.3 CGR formation in BAB7004. CGR presents at least three breakpoint junctions, i.e. Jct1, Jct2, Jct3, which are hypothesized to be generated by template switches during replication-based repair (see main text for discussion). Top: genomic coordinates of junctions inferred from multiple technical approaches. Bottom: representation of the SNP allele dosage in each segment involved in this CGR. A, B: SNP alleles. Genomic coordinates are in hg19

Article Snippet: Structural variation and AOH in subject BAB7004 were identified by clinical chromosome microarray analysis (CMA) using V10.1 OLIGO [ ] which is a custom-designed array with approximately 400,000 interrogating oligonucleotides that include 60,000 probes used for assaying single-nucleotide polymorphisms (SNPs) (Agilent Technologies, Inc., Santa Clara, CA, USA) [ ].

Techniques: Generated