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reference genome ncbi build 36 (hg18)  (Biotechnology Information)

 
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    Biotechnology Information reference genome ncbi build 36 (hg18)
    Segregation of DPP6 in family 1270. Segregation analysis of three rare variants identified in WGS data in intron 1 of DPP6 <t>(hg18</t> variant 1 g.153577081 A>G, variant 2 g.153737600 C>T; rs567013292 and variant 3 g.153744958 G>T) delimited by the STR markers D7S798 and D7S2546. Black bars represent the disease haplotype of patients. Numbers within each diamond are unaffected individuals, non-carriers of the disease haplotype included in the genotyping. Arabic numbers above the symbols denote individuals, Arabic numbers below the symbols denote age at onset for patients or either age at last examination or age at death for unaffected individuals. The arrow identifies the proband in the family. WGS data were generated for patients III-12, III-38, III-41, and III-48 from three different sib ships of the pedigree. Direct long-read WGS on Oxford Nanopore PromethION sequencer was performed for III-48. Directional genomic hybridization was performed in cell lines derived from patient III-48 (Fig. ) and from the non-carriers III-23 and III-39
    Reference Genome Ncbi Build 36 (Hg18), supplied by Biotechnology Information, 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/reference+genome+ncbi+build+36+%28hg18%29/pmc06531610-68-17-12?v=Biotechnology+Information
    Average 90 stars, based on 1 article reviews
    reference genome ncbi build 36 (hg18) - by Bioz Stars, 2026-08
    90/100 stars

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    1) Product Images from "Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability"

    Article Title: Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability

    Journal: Acta Neuropathologica

    doi: 10.1007/s00401-019-01976-3

    Segregation of DPP6 in family 1270. Segregation analysis of three rare variants identified in WGS data in intron 1 of DPP6 (hg18 variant 1 g.153577081 A>G, variant 2 g.153737600 C>T; rs567013292 and variant 3 g.153744958 G>T) delimited by the STR markers D7S798 and D7S2546. Black bars represent the disease haplotype of patients. Numbers within each diamond are unaffected individuals, non-carriers of the disease haplotype included in the genotyping. Arabic numbers above the symbols denote individuals, Arabic numbers below the symbols denote age at onset for patients or either age at last examination or age at death for unaffected individuals. The arrow identifies the proband in the family. WGS data were generated for patients III-12, III-38, III-41, and III-48 from three different sib ships of the pedigree. Direct long-read WGS on Oxford Nanopore PromethION sequencer was performed for III-48. Directional genomic hybridization was performed in cell lines derived from patient III-48 (Fig. ) and from the non-carriers III-23 and III-39
    Figure Legend Snippet: Segregation of DPP6 in family 1270. Segregation analysis of three rare variants identified in WGS data in intron 1 of DPP6 (hg18 variant 1 g.153577081 A>G, variant 2 g.153737600 C>T; rs567013292 and variant 3 g.153744958 G>T) delimited by the STR markers D7S798 and D7S2546. Black bars represent the disease haplotype of patients. Numbers within each diamond are unaffected individuals, non-carriers of the disease haplotype included in the genotyping. Arabic numbers above the symbols denote individuals, Arabic numbers below the symbols denote age at onset for patients or either age at last examination or age at death for unaffected individuals. The arrow identifies the proband in the family. WGS data were generated for patients III-12, III-38, III-41, and III-48 from three different sib ships of the pedigree. Direct long-read WGS on Oxford Nanopore PromethION sequencer was performed for III-48. Directional genomic hybridization was performed in cell lines derived from patient III-48 (Fig. ) and from the non-carriers III-23 and III-39

    Techniques Used: Variant Assay, Generated, Hybridization, Derivative Assay



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    reference genome ncbi build 36 (hg18)  (Biotechnology Information)
    90
    Biotechnology Information reference genome ncbi build 36 (hg18)
    Segregation of DPP6 in family 1270. Segregation analysis of three rare variants identified in WGS data in intron 1 of DPP6 <t>(hg18</t> variant 1 g.153577081 A>G, variant 2 g.153737600 C>T; rs567013292 and variant 3 g.153744958 G>T) delimited by the STR markers D7S798 and D7S2546. Black bars represent the disease haplotype of patients. Numbers within each diamond are unaffected individuals, non-carriers of the disease haplotype included in the genotyping. Arabic numbers above the symbols denote individuals, Arabic numbers below the symbols denote age at onset for patients or either age at last examination or age at death for unaffected individuals. The arrow identifies the proband in the family. WGS data were generated for patients III-12, III-38, III-41, and III-48 from three different sib ships of the pedigree. Direct long-read WGS on Oxford Nanopore PromethION sequencer was performed for III-48. Directional genomic hybridization was performed in cell lines derived from patient III-48 (Fig. ) and from the non-carriers III-23 and III-39
    Reference Genome Ncbi Build 36 (Hg18), supplied by Biotechnology Information, 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/reference+genome+ncbi+build+36+%28hg18%29/pmc06531610-68-17-12?v=Biotechnology+Information
    Average 90 stars, based on 1 article reviews
    reference genome ncbi build 36 (hg18) - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier

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    Segregation of DPP6 in family 1270. Segregation analysis of three rare variants identified in WGS data in intron 1 of DPP6 (hg18 variant 1 g.153577081 A>G, variant 2 g.153737600 C>T; rs567013292 and variant 3 g.153744958 G>T) delimited by the STR markers D7S798 and D7S2546. Black bars represent the disease haplotype of patients. Numbers within each diamond are unaffected individuals, non-carriers of the disease haplotype included in the genotyping. Arabic numbers above the symbols denote individuals, Arabic numbers below the symbols denote age at onset for patients or either age at last examination or age at death for unaffected individuals. The arrow identifies the proband in the family. WGS data were generated for patients III-12, III-38, III-41, and III-48 from three different sib ships of the pedigree. Direct long-read WGS on Oxford Nanopore PromethION sequencer was performed for III-48. Directional genomic hybridization was performed in cell lines derived from patient III-48 (Fig. ) and from the non-carriers III-23 and III-39

    Journal: Acta Neuropathologica

    Article Title: Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability

    doi: 10.1007/s00401-019-01976-3

    Figure Lengend Snippet: Segregation of DPP6 in family 1270. Segregation analysis of three rare variants identified in WGS data in intron 1 of DPP6 (hg18 variant 1 g.153577081 A>G, variant 2 g.153737600 C>T; rs567013292 and variant 3 g.153744958 G>T) delimited by the STR markers D7S798 and D7S2546. Black bars represent the disease haplotype of patients. Numbers within each diamond are unaffected individuals, non-carriers of the disease haplotype included in the genotyping. Arabic numbers above the symbols denote individuals, Arabic numbers below the symbols denote age at onset for patients or either age at last examination or age at death for unaffected individuals. The arrow identifies the proband in the family. WGS data were generated for patients III-12, III-38, III-41, and III-48 from three different sib ships of the pedigree. Direct long-read WGS on Oxford Nanopore PromethION sequencer was performed for III-48. Directional genomic hybridization was performed in cell lines derived from patient III-48 (Fig. ) and from the non-carriers III-23 and III-39

    Article Snippet: Raw sequencing reads were aligned to the reference genome (National Center for Biotechnology Information (NCBI) build 36 (hg18).

    Techniques: Variant Assay, Generated, Hybridization, Derivative Assay