快板版本2。 - Suppr

Suppr

超能文献

Allegro version 2.

作者信息

Gudbjartsson Daniel F, Thorvaldsson Thorvaldur, Kong Augustine, Gunnarsson Gunnar, Ingolfsdottir Anna

出版信息

Nat Genet. 2005 Oct;37(10):1015-6. doi: 10.1038/ng1005-1015.

DOI:10.1038/ng1005-1015

PMID:16195711

Abstract

摘要

相似文献

Allegro version 2.

Nat Genet. 2005 Oct;37(10):1015-6. doi: 10.1038/ng1005-1015.

Allegro, a new computer program for multipoint linkage analysis.

Nat Genet. 2000 May;25(1):12-3. doi: 10.1038/75514.

Estimation of recombination and genetic risks using several markers.

Prog Clin Biol Res. 1984;147:267-9.

The use of grid computing to drive data-intensive genetic research.

Eur J Hum Genet. 2007 Jun;15(6):694-702. doi: 10.1038/sj.ejhg.5201815. Epub 2007 Mar 21.

Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families.

Genomics. 2006 Jan;87(1):1-29. doi: 10.1016/j.ygeno.2005.09.001. Epub 2005 Nov 28.

Family-based methods for linkage and association analysis.

Adv Genet. 2008;60:219-52. doi: 10.1016/S0065-2660(07)00410-5.

On identification problems requiring linked autosomal markers.

Forensic Sci Int Genet. 2008 Jun;2(3):219-25. doi: 10.1016/j.fsigen.2008.02.006. Epub 2008 Apr 18.

AFLP-based genetic linkage maps of the blue mussel (Mytilus edulis).

Anim Genet. 2007 Aug;38(4):340-9. doi: 10.1111/j.1365-2052.2007.01611.x. Epub 2007 Jun 9.

Kinship testing with X-chromosomal markers: mathematical and statistical issues.

Forensic Sci Int Genet. 2007 Jun;1(2):111-4. doi: 10.1016/j.fsigen.2007.01.014. Epub 2007 Feb 27.

LINKAGE programs: linkage analysis for monogenic cardiovascular diseases.

Methods Mol Med. 2006;128:41-60. doi: 10.1385/1-59745-159-2:41.

引用本文的文献

The Variant Causing Autosomal Dominant Deafness in a Nicaraguan Family Enhances Sensitivity to Noise-Induced Hearing Loss in Mice.

medRxiv. 2025 Aug 14:2025.08.13.25333146. doi: 10.1101/2025.08.13.25333146.

Biallelic variants in DNAJC7 cause familial amyotrophic lateral sclerosis with the TDP-43 pathology.

Acta Neuropathol. 2025 Aug 13;150(1):19. doi: 10.1007/s00401-025-02899-y.

Drawing human pedigree charts with DrawPed.

Nucleic Acids Res. 2024 Jul 5;52(W1):W61-W64. doi: 10.1093/nar/gkae336.

Non-syndromic Intellectual Disability: An Experimental In-Depth Exploration of Inheritance Pattern, Phenotypic Presentation, and Genomic Composition.

Cureus. 2023 Jan 23;15(1):e34085. doi: 10.7759/cureus.34085. eCollection 2023 Jan.

SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report.

BMC Neurol. 2021 Feb 11;21(1):64. doi: 10.1186/s12883-021-02087-x.

Alternative Applications of Genotyping Array Data Using Multivariant Methods.

Trends Genet. 2020 Nov;36(11):857-867. doi: 10.1016/j.tig.2020.07.006. Epub 2020 Aug 6.

Crossover interference and sex-specific genetic maps shape identical by descent sharing in close relatives.

PLoS Genet. 2019 Dec 20;15(12):e1007979. doi: 10.1371/journal.pgen.1007979. eCollection 2019 Dec.

Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-Invaginatus.

Front Genet. 2019 Sep 20;10:800. doi: 10.3389/fgene.2019.00800. eCollection 2019.

Atypical Familial Amyotrophic Lateral Sclerosis with Slowly Progressing Lower Extremities-predominant Late-onset Muscular Weakness and Atrophy.

Intern Med. 2019;58(13):1851-1858. doi: 10.2169/internalmedicine.2222-18. Epub 2019 Jul 1.

Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability.

Hum Genet. 2018 Sep;137(9):735-752. doi: 10.1007/s00439-018-1928-6. Epub 2018 Aug 22.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

Allegro version 2.

作者信息

Gudbjartsson Daniel F, Thorvaldsson Thorvaldur, Kong Augustine, Gunnarsson Gunnar, Ingolfsdottir Anna

出版信息

Nat Genet. 2005 Oct;37(10):1015-6. doi: 10.1038/ng1005-1015.

DOI:10.1038/ng1005-1015

PMID:16195711

Abstract

摘要

相似文献

Allegro version 2.

Nat Genet. 2005 Oct;37(10):1015-6. doi: 10.1038/ng1005-1015.

Allegro, a new computer program for multipoint linkage analysis.

Nat Genet. 2000 May;25(1):12-3. doi: 10.1038/75514.

Estimation of recombination and genetic risks using several markers.

Prog Clin Biol Res. 1984;147:267-9.

The use of grid computing to drive data-intensive genetic research.

Eur J Hum Genet. 2007 Jun;15(6):694-702. doi: 10.1038/sj.ejhg.5201815. Epub 2007 Mar 21.

Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families.

Genomics. 2006 Jan;87(1):1-29. doi: 10.1016/j.ygeno.2005.09.001. Epub 2005 Nov 28.

Family-based methods for linkage and association analysis.

Adv Genet. 2008;60:219-52. doi: 10.1016/S0065-2660(07)00410-5.

On identification problems requiring linked autosomal markers.

Forensic Sci Int Genet. 2008 Jun;2(3):219-25. doi: 10.1016/j.fsigen.2008.02.006. Epub 2008 Apr 18.

AFLP-based genetic linkage maps of the blue mussel (Mytilus edulis).

Anim Genet. 2007 Aug;38(4):340-9. doi: 10.1111/j.1365-2052.2007.01611.x. Epub 2007 Jun 9.

Kinship testing with X-chromosomal markers: mathematical and statistical issues.

Forensic Sci Int Genet. 2007 Jun;1(2):111-4. doi: 10.1016/j.fsigen.2007.01.014. Epub 2007 Feb 27.

LINKAGE programs: linkage analysis for monogenic cardiovascular diseases.

Methods Mol Med. 2006;128:41-60. doi: 10.1385/1-59745-159-2:41.

引用本文的文献

The Variant Causing Autosomal Dominant Deafness in a Nicaraguan Family Enhances Sensitivity to Noise-Induced Hearing Loss in Mice.

medRxiv. 2025 Aug 14:2025.08.13.25333146. doi: 10.1101/2025.08.13.25333146.

Biallelic variants in DNAJC7 cause familial amyotrophic lateral sclerosis with the TDP-43 pathology.

Acta Neuropathol. 2025 Aug 13;150(1):19. doi: 10.1007/s00401-025-02899-y.

Drawing human pedigree charts with DrawPed.

Nucleic Acids Res. 2024 Jul 5;52(W1):W61-W64. doi: 10.1093/nar/gkae336.

Non-syndromic Intellectual Disability: An Experimental In-Depth Exploration of Inheritance Pattern, Phenotypic Presentation, and Genomic Composition.

Cureus. 2023 Jan 23;15(1):e34085. doi: 10.7759/cureus.34085. eCollection 2023 Jan.

SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report.

BMC Neurol. 2021 Feb 11;21(1):64. doi: 10.1186/s12883-021-02087-x.

Alternative Applications of Genotyping Array Data Using Multivariant Methods.

Trends Genet. 2020 Nov;36(11):857-867. doi: 10.1016/j.tig.2020.07.006. Epub 2020 Aug 6.

Crossover interference and sex-specific genetic maps shape identical by descent sharing in close relatives.

PLoS Genet. 2019 Dec 20;15(12):e1007979. doi: 10.1371/journal.pgen.1007979. eCollection 2019 Dec.

Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-Invaginatus.

Front Genet. 2019 Sep 20;10:800. doi: 10.3389/fgene.2019.00800. eCollection 2019.

Atypical Familial Amyotrophic Lateral Sclerosis with Slowly Progressing Lower Extremities-predominant Late-onset Muscular Weakness and Atrophy.

Intern Med. 2019;58(13):1851-1858. doi: 10.2169/internalmedicine.2222-18. Epub 2019 Jul 1.

Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability.

Hum Genet. 2018 Sep;137(9):735-752. doi: 10.1007/s00439-018-1928-6. Epub 2018 Aug 22.