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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1943 1
1945 4
1946 16
1947 14
1948 31
1949 15
1950 29
1951 45
1952 24
1953 35
1954 44
1955 35
1956 55
1957 52
1958 45
1959 53
1960 55
1961 62
1962 52
1963 75
1964 86
1965 37
1966 41
1967 286
1968 533
1969 617
1970 692
1971 941
1972 1138
1973 1263
1974 1777
1975 1400
1976 1162
1977 1039
1978 881
1979 949
1980 828
1981 841
1982 974
1983 931
1984 1175
1985 1134
1986 1263
1987 1425
1988 1419
1989 1799
1990 2205
1991 2289
1992 2430
1993 2802
1994 3415
1995 4124
1996 4602
1997 5459
1998 6194
1999 7749
2000 9150
2001 10502
2002 10735
2003 11975
2004 13666
2005 15645
2006 16653
2007 18617
2008 20871
2009 22236
2010 23684
2011 24843
2012 25898
2013 26018
2014 25814
2015 25683
2016 24698
2017 23111
2018 20595
2019 10112
2020 251
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402,793 results
Results by year
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Page 1
Next-generation genotype imputation service and methods.
Das S, et al. Nat Genet 2016. PMID 27571263 Free PMC article.
Genotype imputation is a key component of genetic association studies, where it increases power, facilitates meta-analysis, and aids interpretation of signals. Genotype imputation is computationally demanding and, with current tools, typically requires access to a high-performance computing cluster and to a reference panel of sequenced genomes. ...
Genotype imputation is a key component of genetic association studies, where it increases power, facilitates meta-analysis, and aids
Haplotype Inference
Song S, et al. Methods Mol Biol 2017. PMID 28980260
In this chapter, we introduce four representative methods to reconstruct haplotypes from unphased genotype data, two of them are for unrelated individuals and the other two are for families....
In this chapter, we introduce four representative methods to reconstruct haplotypes from unphased genotype data, two of them are for …
Mechanisms of Mendelian dominance
Veitia RA, et al. Clin Genet 2018 - Review. PMID 28755412
BCFtools/RoH: a hidden Markov model approach for detecting autozygosity from next-generation sequencing data
Narasimhan V, et al. Bioinformatics 2016. PMID 26826718 Free PMC article.
Early tools to detect RoH used genotype array data, but substantially more information is available from sequencing data. Here, we present and evaluate BCFtools/RoH, an extension to the BCFtools software package, that detects regions of autozygosity in sequencing data, in particular exome data, using a hidden Markov model. ...
Early tools to detect RoH used genotype array data, but substantially more information is available from sequencing data. Here, we pr …
402,793 results
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