Індэл (Belarusian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Індэл" in Belarusian language version.

refsWebsite

Global rank Belarusian rank

24nih.gov

4^th place

66^th place

15doi.org

2^nd place

22^nd place

3harvard.edu

18^th place

75^th place

2semanticscholar.org

11^th place

3,063^rd place

1science.org

1,160^th place

low place

1worldcat.org

5^th place

13^th place

doi.org

Mahmoud, Medhat; Gobet, Nastassia; Cruz-Dávalos, Diana Ivette; Mounier, Ninon; Dessimoz, Christophe; Sedlazeck, Fritz J. (2019). "Structural variant calling: the long and the short of it". Genome Biology. 20. doi:10.1186/s13059-019-1828-7. PMC 6868818.
Ebert, Peter; et al. (2021). "Haplotype-resolved diverse human genomes and integrated analysis of structural variation". Science. 372 (6537). doi:10.1126/science.abf7117. PMC 8026704.
Kaneko T, Tahara S, Matsuo M (May 1996). "Non-linear accumulation of 8-hydroxy-2'-deoxyguanosine, a marker of oxidized DNA damage, during aging". Mutation Research. 316 (5–6): 277–285. doi:10.1016/S0921-8734(96)90010-7. PMID 8649461.
Hill KA, Wang J, Farwell KD, Sommer SS (January 2003). "Spontaneous tandem-base mutations (TBM) show dramatic tissue, age, pattern and spectrum specificity". Mutation Research. 534 (1–2): 173–186. doi:10.1016/S1383-5718(02)00277-2. PMID 12504766.
Buettner VL, Hill KA, Halangoda A, Sommer SS (1999). "Tandem-base mutations occur in mouse liver and adipose tissue preferentially as G:C to T:A transversions and accumulate with age". Environmental and Molecular Mutagenesis. 33 (4): 320–324. doi:10.1002/(SICI)1098-2280(1999)33:4<320::AID-EM9>3.0.CO;2-S. PMID 10398380. S2CID 37019230.
Väli U, Brandström M, Johansson M, Ellegren H (January 2008). "Insertion-deletion polymorphisms (indels) as genetic markers in natural populations". BMC Genetics. 9: 8. doi:10.1186/1471-2156-9-8. PMC 2266919. PMID 18211670.
Erixon P, Oxelman B (January 2008). Volff JN (рэд.). "Whole-gene positive selection, elevated synonymous substitution rates, duplication, and indel evolution of the chloroplast clpP1 gene". PLOS ONE. 3 (1): e1386. Bibcode:2008PLoSO...3.1386E. doi:10.1371/journal.pone.0001386. PMC 2148103. PMID 18167545.
Pereira F, Carneiro J, Matthiesen R, van Asch B, Pinto N, Gusmão L, Amorim A (December 2010). "Identification of species by multiplex analysis of variable-length sequences". Nucleic Acids Research. 38 (22): e203. doi:10.1093/nar/gkq865. PMC 3001097. PMID 20923781.
Nakamura H, Muro T, Imamura S, Yuasa I (March 2009). "Forensic species identification based on size variation of mitochondrial DNA hypervariable regions". International Journal of Legal Medicine. 123 (2): 177–184. doi:10.1007/s00414-008-0306-7. PMID 19052767. S2CID 10531572.
Taberlet P, Coissac E, Pompanon F, Gielly L, Miquel C, Valentini A, et al. (26 January 2007). "Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding". Nucleic Acids Research. 35 (3): e14. doi:10.1093/nar/gkl938. PMC 1807943. PMID 17169982.
Bai H, Cao Y, Quan J, Dong L, Li Z, Zhu Y, et al. (2013). "Identifying the genome-wide sequence variations and developing new molecular markers for genetics research by re-sequencing a Landrace cultivar of foxtail millet". PLOS ONE. 8 (9): e73514. Bibcode:2013PLoSO...873514B. doi:10.1371/journal.pone.0073514. PMC 3769310. PMID 24039970.
Zheng LY, Guo XS, He B, Sun LJ, Peng Y, Dong SS, et al. (November 2011). "Genome-wide patterns of genetic variation in sweet and grain sorghum (Sorghum bicolor)". Genome Biology. 12 (11): R114. doi:10.1186/gb-2011-12-11-r114. PMC 3334600. PMID 22104744.
Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, et al. (October 2010). "A map of human genome variation from population-scale sequencing". Nature. 467 (7319): 1061–1073. Bibcode:2010Natur.467.1061T. doi:10.1038/nature09534. PMC 3042601. PMID 20981092.
Mills RE, Luttig CT, Larkins CE, Beauchamp A, Tsui C, Pittard WS, Devine SE (September 2006). "An initial map of insertion and deletion (INDEL) variation in the human genome". Genome Research. 16 (9): 1182–1190. doi:10.1101/gr.4565806. PMC 1557762. PMID 16902084.
Hao, Qian; Zhan, Chuanzong; Lian, Chaoyang; Luo, Simin; Cao, Wenyi; Wang, Binbin; Xie, Xia; Ye, Xiaofei; Gui, Tuantuan; Voena, Claudia; Pighi, Chiara; Wang, Yanyan; Tian, Ying; Wang, Xin; Dai, Pengfei (2023-03-31). "DNA repair mechanisms that promote insertion-deletion events during immunoglobulin gene diversification". Science Immunology(англ.). 8 (81): eade1167. doi:10.1126/sciimmunol.ade1167. ISSN 2470-9468. PMC 10351598. PMID 36961908.

harvard.edu

ui.adsabs.harvard.edu

Erixon P, Oxelman B (January 2008). Volff JN (рэд.). "Whole-gene positive selection, elevated synonymous substitution rates, duplication, and indel evolution of the chloroplast clpP1 gene". PLOS ONE. 3 (1): e1386. Bibcode:2008PLoSO...3.1386E. doi:10.1371/journal.pone.0001386. PMC 2148103. PMID 18167545.
Bai H, Cao Y, Quan J, Dong L, Li Z, Zhu Y, et al. (2013). "Identifying the genome-wide sequence variations and developing new molecular markers for genetics research by re-sequencing a Landrace cultivar of foxtail millet". PLOS ONE. 8 (9): e73514. Bibcode:2013PLoSO...873514B. doi:10.1371/journal.pone.0073514. PMC 3769310. PMID 24039970.
Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, et al. (October 2010). "A map of human genome variation from population-scale sequencing". Nature. 467 (7319): 1061–1073. Bibcode:2010Natur.467.1061T. doi:10.1038/nature09534. PMC 3042601. PMID 20981092.

nih.gov

pubmed.ncbi.nlm.nih.gov

Kaneko T, Tahara S, Matsuo M (May 1996). "Non-linear accumulation of 8-hydroxy-2'-deoxyguanosine, a marker of oxidized DNA damage, during aging". Mutation Research. 316 (5–6): 277–285. doi:10.1016/S0921-8734(96)90010-7. PMID 8649461.
Hill KA, Wang J, Farwell KD, Sommer SS (January 2003). "Spontaneous tandem-base mutations (TBM) show dramatic tissue, age, pattern and spectrum specificity". Mutation Research. 534 (1–2): 173–186. doi:10.1016/S1383-5718(02)00277-2. PMID 12504766.
Buettner VL, Hill KA, Halangoda A, Sommer SS (1999). "Tandem-base mutations occur in mouse liver and adipose tissue preferentially as G:C to T:A transversions and accumulate with age". Environmental and Molecular Mutagenesis. 33 (4): 320–324. doi:10.1002/(SICI)1098-2280(1999)33:4<320::AID-EM9>3.0.CO;2-S. PMID 10398380. S2CID 37019230.
Väli U, Brandström M, Johansson M, Ellegren H (January 2008). "Insertion-deletion polymorphisms (indels) as genetic markers in natural populations". BMC Genetics. 9: 8. doi:10.1186/1471-2156-9-8. PMC 2266919. PMID 18211670.
Erixon P, Oxelman B (January 2008). Volff JN (рэд.). "Whole-gene positive selection, elevated synonymous substitution rates, duplication, and indel evolution of the chloroplast clpP1 gene". PLOS ONE. 3 (1): e1386. Bibcode:2008PLoSO...3.1386E. doi:10.1371/journal.pone.0001386. PMC 2148103. PMID 18167545.
Pereira F, Carneiro J, Matthiesen R, van Asch B, Pinto N, Gusmão L, Amorim A (December 2010). "Identification of species by multiplex analysis of variable-length sequences". Nucleic Acids Research. 38 (22): e203. doi:10.1093/nar/gkq865. PMC 3001097. PMID 20923781.
Nakamura H, Muro T, Imamura S, Yuasa I (March 2009). "Forensic species identification based on size variation of mitochondrial DNA hypervariable regions". International Journal of Legal Medicine. 123 (2): 177–184. doi:10.1007/s00414-008-0306-7. PMID 19052767. S2CID 10531572.
Taberlet P, Coissac E, Pompanon F, Gielly L, Miquel C, Valentini A, et al. (26 January 2007). "Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding". Nucleic Acids Research. 35 (3): e14. doi:10.1093/nar/gkl938. PMC 1807943. PMID 17169982.
Bai H, Cao Y, Quan J, Dong L, Li Z, Zhu Y, et al. (2013). "Identifying the genome-wide sequence variations and developing new molecular markers for genetics research by re-sequencing a Landrace cultivar of foxtail millet". PLOS ONE. 8 (9): e73514. Bibcode:2013PLoSO...873514B. doi:10.1371/journal.pone.0073514. PMC 3769310. PMID 24039970.
Zheng LY, Guo XS, He B, Sun LJ, Peng Y, Dong SS, et al. (November 2011). "Genome-wide patterns of genetic variation in sweet and grain sorghum (Sorghum bicolor)". Genome Biology. 12 (11): R114. doi:10.1186/gb-2011-12-11-r114. PMC 3334600. PMID 22104744.
Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, et al. (October 2010). "A map of human genome variation from population-scale sequencing". Nature. 467 (7319): 1061–1073. Bibcode:2010Natur.467.1061T. doi:10.1038/nature09534. PMC 3042601. PMID 20981092.
Mills RE, Luttig CT, Larkins CE, Beauchamp A, Tsui C, Pittard WS, Devine SE (September 2006). "An initial map of insertion and deletion (INDEL) variation in the human genome". Genome Research. 16 (9): 1182–1190. doi:10.1101/gr.4565806. PMC 1557762. PMID 16902084.
Hao, Qian; Zhan, Chuanzong; Lian, Chaoyang; Luo, Simin; Cao, Wenyi; Wang, Binbin; Xie, Xia; Ye, Xiaofei; Gui, Tuantuan; Voena, Claudia; Pighi, Chiara; Wang, Yanyan; Tian, Ying; Wang, Xin; Dai, Pengfei (2023-03-31). "DNA repair mechanisms that promote insertion-deletion events during immunoglobulin gene diversification". Science Immunology(англ.). 8 (81): eade1167. doi:10.1126/sciimmunol.ade1167. ISSN 2470-9468. PMC 10351598. PMID 36961908.

ncbi.nlm.nih.gov

Mahmoud, Medhat; Gobet, Nastassia; Cruz-Dávalos, Diana Ivette; Mounier, Ninon; Dessimoz, Christophe; Sedlazeck, Fritz J. (2019). "Structural variant calling: the long and the short of it". Genome Biology. 20. doi:10.1186/s13059-019-1828-7. PMC 6868818.
Ebert, Peter; et al. (2021). "Haplotype-resolved diverse human genomes and integrated analysis of structural variation". Science. 372 (6537). doi:10.1126/science.abf7117. PMC 8026704.
Väli U, Brandström M, Johansson M, Ellegren H (January 2008). "Insertion-deletion polymorphisms (indels) as genetic markers in natural populations". BMC Genetics. 9: 8. doi:10.1186/1471-2156-9-8. PMC 2266919. PMID 18211670.
Erixon P, Oxelman B (January 2008). Volff JN (рэд.). "Whole-gene positive selection, elevated synonymous substitution rates, duplication, and indel evolution of the chloroplast clpP1 gene". PLOS ONE. 3 (1): e1386. Bibcode:2008PLoSO...3.1386E. doi:10.1371/journal.pone.0001386. PMC 2148103. PMID 18167545.
Pereira F, Carneiro J, Matthiesen R, van Asch B, Pinto N, Gusmão L, Amorim A (December 2010). "Identification of species by multiplex analysis of variable-length sequences". Nucleic Acids Research. 38 (22): e203. doi:10.1093/nar/gkq865. PMC 3001097. PMID 20923781.
Taberlet P, Coissac E, Pompanon F, Gielly L, Miquel C, Valentini A, et al. (26 January 2007). "Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding". Nucleic Acids Research. 35 (3): e14. doi:10.1093/nar/gkl938. PMC 1807943. PMID 17169982.
Bai H, Cao Y, Quan J, Dong L, Li Z, Zhu Y, et al. (2013). "Identifying the genome-wide sequence variations and developing new molecular markers for genetics research by re-sequencing a Landrace cultivar of foxtail millet". PLOS ONE. 8 (9): e73514. Bibcode:2013PLoSO...873514B. doi:10.1371/journal.pone.0073514. PMC 3769310. PMID 24039970.
Zheng LY, Guo XS, He B, Sun LJ, Peng Y, Dong SS, et al. (November 2011). "Genome-wide patterns of genetic variation in sweet and grain sorghum (Sorghum bicolor)". Genome Biology. 12 (11): R114. doi:10.1186/gb-2011-12-11-r114. PMC 3334600. PMID 22104744.
Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, et al. (October 2010). "A map of human genome variation from population-scale sequencing". Nature. 467 (7319): 1061–1073. Bibcode:2010Natur.467.1061T. doi:10.1038/nature09534. PMC 3042601. PMID 20981092.
Mills RE, Luttig CT, Larkins CE, Beauchamp A, Tsui C, Pittard WS, Devine SE (September 2006). "An initial map of insertion and deletion (INDEL) variation in the human genome". Genome Research. 16 (9): 1182–1190. doi:10.1101/gr.4565806. PMC 1557762. PMID 16902084.
Hao, Qian; Zhan, Chuanzong; Lian, Chaoyang; Luo, Simin; Cao, Wenyi; Wang, Binbin; Xie, Xia; Ye, Xiaofei; Gui, Tuantuan; Voena, Claudia; Pighi, Chiara; Wang, Yanyan; Tian, Ying; Wang, Xin; Dai, Pengfei (2023-03-31). "DNA repair mechanisms that promote insertion-deletion events during immunoglobulin gene diversification". Science Immunology(англ.). 8 (81): eade1167. doi:10.1126/sciimmunol.ade1167. ISSN 2470-9468. PMC 10351598. PMID 36961908.

science.org

Ebert, Peter; et al. (2021). "Haplotype-resolved diverse human genomes and integrated analysis of structural variation". Science. 372 (6537). doi:10.1126/science.abf7117. PMC 8026704.

semanticscholar.org

api.semanticscholar.org

Buettner VL, Hill KA, Halangoda A, Sommer SS (1999). "Tandem-base mutations occur in mouse liver and adipose tissue preferentially as G:C to T:A transversions and accumulate with age". Environmental and Molecular Mutagenesis. 33 (4): 320–324. doi:10.1002/(SICI)1098-2280(1999)33:4<320::AID-EM9>3.0.CO;2-S. PMID 10398380. S2CID 37019230.
Nakamura H, Muro T, Imamura S, Yuasa I (March 2009). "Forensic species identification based on size variation of mitochondrial DNA hypervariable regions". International Journal of Legal Medicine. 123 (2): 177–184. doi:10.1007/s00414-008-0306-7. PMID 19052767. S2CID 10531572.

worldcat.org

Hao, Qian; Zhan, Chuanzong; Lian, Chaoyang; Luo, Simin; Cao, Wenyi; Wang, Binbin; Xie, Xia; Ye, Xiaofei; Gui, Tuantuan; Voena, Claudia; Pighi, Chiara; Wang, Yanyan; Tian, Ying; Wang, Xin; Dai, Pengfei (2023-03-31). "DNA repair mechanisms that promote insertion-deletion events during immunoglobulin gene diversification". Science Immunology(англ.). 8 (81): eade1167. doi:10.1126/sciimmunol.ade1167. ISSN 2470-9468. PMC 10351598. PMID 36961908.