snv Search Results


92
Thermo Fisher snv rs10069690
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Thermo Fisher snv nlpr3 rs10754558
Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.
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Thermo Fisher snv nlpr3 rs10157379
Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.
Snv Nlpr3 Rs10157379, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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EUROIMMUN biochip containing infected and non-infected vero e6 cells or only non-infected vero e6 cells (negative control)
Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.
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PharmaJet Inc lnp-formulated andv dna vaccine
Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.
Lnp Formulated Andv Dna Vaccine, supplied by PharmaJet 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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NanoVector silicon nanovector snv
Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.
Silicon Nanovector Snv, supplied by NanoVector, 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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Great Basin Corp snv sequence
Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.
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Ridom GmbH snv tool implemented in seqsphere
Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.
Snv Tool Implemented In Seqsphere, supplied by Ridom GmbH, 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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MultiTarget Pharmaceuticals ar multiplex snv assay l702h-w742l/c
Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.
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Broad Institute Inc snv data broad2
Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.
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CLC Bio snv detection tools
Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.
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SourceForge net qq-snv
SNVs called by <t> QQ-SNV </t> HS-P80 on H1N1 clinical sample (all paired-end reads)
Qq Snv, supplied by SourceForge net, 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


Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.

Journal: Molecular Psychiatry

Article Title: In COVID-19, NLRP3 inflammasome genetic variants are associated with critical disease and these effects are partly mediated by the sickness symptom complex: a nomothetic network approach

doi: 10.1038/s41380-021-01431-4

Figure Lengend Snippet: Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.

Article Snippet: Real-time polymerase chain reaction (qPCR) with the TaqMan® (Thermo Fisher Scientific, Waltham, Massachusetts, EUA) method was used to identify SNV NLPR3 rs10157379 (T > C) and SNV NLPR3 rs10754558 (C > G) variants.

Techniques:

Results of binary logistic regression analysis with clinical outcomes as dependent variables.

Journal: Molecular Psychiatry

Article Title: In COVID-19, NLRP3 inflammasome genetic variants are associated with critical disease and these effects are partly mediated by the sickness symptom complex: a nomothetic network approach

doi: 10.1038/s41380-021-01431-4

Figure Lengend Snippet: Results of binary logistic regression analysis with clinical outcomes as dependent variables.

Article Snippet: Real-time polymerase chain reaction (qPCR) with the TaqMan® (Thermo Fisher Scientific, Waltham, Massachusetts, EUA) method was used to identify SNV NLPR3 rs10157379 (T > C) and SNV NLPR3 rs10754558 (C > G) variants.

Techniques:

Results of multiple regression analyses with symptoms profiles and high-risk indices as dependent variables.

Journal: Molecular Psychiatry

Article Title: In COVID-19, NLRP3 inflammasome genetic variants are associated with critical disease and these effects are partly mediated by the sickness symptom complex: a nomothetic network approach

doi: 10.1038/s41380-021-01431-4

Figure Lengend Snippet: Results of multiple regression analyses with symptoms profiles and high-risk indices as dependent variables.

Article Snippet: Real-time polymerase chain reaction (qPCR) with the TaqMan® (Thermo Fisher Scientific, Waltham, Massachusetts, EUA) method was used to identify SNV NLPR3 rs10157379 (T > C) and SNV NLPR3 rs10754558 (C > G) variants.

Techniques:

Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.

Journal: Molecular Psychiatry

Article Title: In COVID-19, NLRP3 inflammasome genetic variants are associated with critical disease and these effects are partly mediated by the sickness symptom complex: a nomothetic network approach

doi: 10.1038/s41380-021-01431-4

Figure Lengend Snippet: Associations between NLRP3 inflammasome genetic variants and symptoms of severe acute respiratory syndrome (SARS) and sickness behavior.

Article Snippet: Real-time polymerase chain reaction (qPCR) with the TaqMan® (Thermo Fisher Scientific, Waltham, Massachusetts, EUA) method was used to identify SNV NLPR3 rs10157379 (T > C) and SNV NLPR3 rs10754558 (C > G) variants.

Techniques:

Results of binary logistic regression analysis with clinical outcomes as dependent variables.

Journal: Molecular Psychiatry

Article Title: In COVID-19, NLRP3 inflammasome genetic variants are associated with critical disease and these effects are partly mediated by the sickness symptom complex: a nomothetic network approach

doi: 10.1038/s41380-021-01431-4

Figure Lengend Snippet: Results of binary logistic regression analysis with clinical outcomes as dependent variables.

Article Snippet: Real-time polymerase chain reaction (qPCR) with the TaqMan® (Thermo Fisher Scientific, Waltham, Massachusetts, EUA) method was used to identify SNV NLPR3 rs10157379 (T > C) and SNV NLPR3 rs10754558 (C > G) variants.

Techniques:

Results of multiple regression analyses with symptoms profiles and high-risk indices as dependent variables.

Journal: Molecular Psychiatry

Article Title: In COVID-19, NLRP3 inflammasome genetic variants are associated with critical disease and these effects are partly mediated by the sickness symptom complex: a nomothetic network approach

doi: 10.1038/s41380-021-01431-4

Figure Lengend Snippet: Results of multiple regression analyses with symptoms profiles and high-risk indices as dependent variables.

Article Snippet: Real-time polymerase chain reaction (qPCR) with the TaqMan® (Thermo Fisher Scientific, Waltham, Massachusetts, EUA) method was used to identify SNV NLPR3 rs10157379 (T > C) and SNV NLPR3 rs10754558 (C > G) variants.

Techniques:

SNVs called by  QQ-SNV  HS-P80 on H1N1 clinical sample (all paired-end reads)

Journal: BMC Bioinformatics

Article Title: QQ-SNV: single nucleotide variant detection at low frequency by comparing the quality quantiles

doi: 10.1186/s12859-015-0812-9

Figure Lengend Snippet: SNVs called by QQ-SNV HS-P80 on H1N1 clinical sample (all paired-end reads)

Article Snippet: Here we present QQ-SNV ( http://sourceforge.net/projects/qqsnv ), a logistic regression classifier model developed for the Illumina sequencing platforms that uses the quantiles of the quality scores, to distinguish true single nucleotide variants from sequencing errors based on the estimated SNV probability.

Techniques: