Additional file 1 of Fragmented mitochondrial genomes of seal lice (family Echinophthiriidae) and gorilla louse (family Pthiridae): frequent minichromosomal splits and a host switch of lice between seals ...
Additional file 1: Supplementary Fig. 1. Secondary structure inferred with tRNA-Scan [33] from trnW1 and trnW2 gene sequences of the southern elephant seal louse, Lepidophthirus macrorhini. Supplementary Fig. 2. Conserved non-coding AT-rich motifs and GC-rich motifs among the mitochondrial minichrom...
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Online Access: | https://dx.doi.org/10.6084/m9.figshare.19565859 https://springernature.figshare.com/articles/journal_contribution/Additional_file_1_of_Fragmented_mitochondrial_genomes_of_seal_lice_family_Echinophthiriidae_and_gorilla_louse_family_Pthiridae_frequent_minichromosomal_splits_and_a_host_switch_of_lice_between_seals/19565859 |
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ftdatacite:10.6084/m9.figshare.19565859 2024-03-31T07:49:18+00:00 Additional file 1 of Fragmented mitochondrial genomes of seal lice (family Echinophthiriidae) and gorilla louse (family Pthiridae): frequent minichromosomal splits and a host switch of lice between seals ... Dong, Yalun Zhao, Min Shao, Renfu 2022 https://dx.doi.org/10.6084/m9.figshare.19565859 https://springernature.figshare.com/articles/journal_contribution/Additional_file_1_of_Fragmented_mitochondrial_genomes_of_seal_lice_family_Echinophthiriidae_and_gorilla_louse_family_Pthiridae_frequent_minichromosomal_splits_and_a_host_switch_of_lice_between_seals/19565859 unknown figshare https://dx.doi.org/10.1093/sysbio/syaa075 https://dx.doi.org/10.1111/j.1365-3113.1978.tb00120.x https://dx.doi.org/10.1093/nar/27.8.1767 https://dx.doi.org/10.1101/gr.083188.108 https://dx.doi.org/10.1093/gbe/evs088 https://dx.doi.org/10.1186/1756-3305-7-144 https://dx.doi.org/10.1093/gbe/evx007 https://dx.doi.org/10.1093/gbe/evt094 https://dx.doi.org/10.1186/1471-2164-15-751 https://dx.doi.org/10.1186/1471-2164-15-44 https://dx.doi.org/10.1016/j.ygeno.2020.09.005 https://dx.doi.org/10.1186/s12864-021-07859-w https://dx.doi.org/10.1186/s12864-015-1843-3 https://dx.doi.org/10.1111/syen.12350 https://dx.doi.org/10.1186/1741-7007-5-7 https://dx.doi.org/10.1007/s00300-015-1822-9 https://dx.doi.org/10.1007/s00436-014-4058-7 https://dx.doi.org/10.1126/science.8066445 https://dx.doi.org/10.1006/mpev.1997.0458 https://dx.doi.org/10.1080/10635159950127303 Creative Commons Attribution 4.0 International https://creativecommons.org/licenses/by/4.0/legalcode cc-by-4.0 Genetics FOS Biological sciences Text Journal contribution article-journal ScholarlyArticle 2022 ftdatacite https://doi.org/10.6084/m9.figshare.1956585910.1093/sysbio/syaa07510.1111/j.1365-3113.1978.tb00120.x10.1093/nar/27.8.176710.1101/gr.083188.10810.1093/gbe/evs08810.1186/1756-3305-7-14410.1093/gbe/evx00710.1093/gbe/evt09410.1186/1471-2164-15-75110.1186/1471 2024-03-04T13:05:49Z Additional file 1: Supplementary Fig. 1. Secondary structure inferred with tRNA-Scan [33] from trnW1 and trnW2 gene sequences of the southern elephant seal louse, Lepidophthirus macrorhini. Supplementary Fig. 2. Conserved non-coding AT-rich motifs and GC-rich motifs among the mitochondrial minichromosomes of the southern elephant seal louse, Lepidophthirus macrorhini. Supplementary Fig. 3. Conserved non-coding AT-rich motifs and GC-rich motifs among the mitochondrial minichromosomes of the northern fur seal louse, Proechinophthirus fluctus. Supplementary Fig. 4. Conserved non-coding AT-rich motifs and GC-rich motifs among the mitochondrial minichromosomes of the Weddell seal louse, Antarctophthirus carlinii. Supplementary Fig. 5. Conserved non-coding AT-rich motifs and GC-rich motifs among the mitochondrial minichromosomes of the crabeater seal louse, Antarctophthirus lobodontis. Supplementary Fig. 6. Conserved non-coding GC-rich motifs among the mitochondrial minichromosomes of the Australian sea lion ... Text Antarc* Crabeater Seal Elephant Seal Southern Elephant Seal Weddell Seal Northern fur seal DataCite Metadata Store (German National Library of Science and Technology) Weddell |
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DataCite Metadata Store (German National Library of Science and Technology) |
op_collection_id |
ftdatacite |
language |
unknown |
topic |
Genetics FOS Biological sciences |
spellingShingle |
Genetics FOS Biological sciences Dong, Yalun Zhao, Min Shao, Renfu Additional file 1 of Fragmented mitochondrial genomes of seal lice (family Echinophthiriidae) and gorilla louse (family Pthiridae): frequent minichromosomal splits and a host switch of lice between seals ... |
topic_facet |
Genetics FOS Biological sciences |
description |
Additional file 1: Supplementary Fig. 1. Secondary structure inferred with tRNA-Scan [33] from trnW1 and trnW2 gene sequences of the southern elephant seal louse, Lepidophthirus macrorhini. Supplementary Fig. 2. Conserved non-coding AT-rich motifs and GC-rich motifs among the mitochondrial minichromosomes of the southern elephant seal louse, Lepidophthirus macrorhini. Supplementary Fig. 3. Conserved non-coding AT-rich motifs and GC-rich motifs among the mitochondrial minichromosomes of the northern fur seal louse, Proechinophthirus fluctus. Supplementary Fig. 4. Conserved non-coding AT-rich motifs and GC-rich motifs among the mitochondrial minichromosomes of the Weddell seal louse, Antarctophthirus carlinii. Supplementary Fig. 5. Conserved non-coding AT-rich motifs and GC-rich motifs among the mitochondrial minichromosomes of the crabeater seal louse, Antarctophthirus lobodontis. Supplementary Fig. 6. Conserved non-coding GC-rich motifs among the mitochondrial minichromosomes of the Australian sea lion ... |
format |
Text |
author |
Dong, Yalun Zhao, Min Shao, Renfu |
author_facet |
Dong, Yalun Zhao, Min Shao, Renfu |
author_sort |
Dong, Yalun |
title |
Additional file 1 of Fragmented mitochondrial genomes of seal lice (family Echinophthiriidae) and gorilla louse (family Pthiridae): frequent minichromosomal splits and a host switch of lice between seals ... |
title_short |
Additional file 1 of Fragmented mitochondrial genomes of seal lice (family Echinophthiriidae) and gorilla louse (family Pthiridae): frequent minichromosomal splits and a host switch of lice between seals ... |
title_full |
Additional file 1 of Fragmented mitochondrial genomes of seal lice (family Echinophthiriidae) and gorilla louse (family Pthiridae): frequent minichromosomal splits and a host switch of lice between seals ... |
title_fullStr |
Additional file 1 of Fragmented mitochondrial genomes of seal lice (family Echinophthiriidae) and gorilla louse (family Pthiridae): frequent minichromosomal splits and a host switch of lice between seals ... |
title_full_unstemmed |
Additional file 1 of Fragmented mitochondrial genomes of seal lice (family Echinophthiriidae) and gorilla louse (family Pthiridae): frequent minichromosomal splits and a host switch of lice between seals ... |
title_sort |
additional file 1 of fragmented mitochondrial genomes of seal lice (family echinophthiriidae) and gorilla louse (family pthiridae): frequent minichromosomal splits and a host switch of lice between seals ... |
publisher |
figshare |
publishDate |
2022 |
url |
https://dx.doi.org/10.6084/m9.figshare.19565859 https://springernature.figshare.com/articles/journal_contribution/Additional_file_1_of_Fragmented_mitochondrial_genomes_of_seal_lice_family_Echinophthiriidae_and_gorilla_louse_family_Pthiridae_frequent_minichromosomal_splits_and_a_host_switch_of_lice_between_seals/19565859 |
geographic |
Weddell |
geographic_facet |
Weddell |
genre |
Antarc* Crabeater Seal Elephant Seal Southern Elephant Seal Weddell Seal Northern fur seal |
genre_facet |
Antarc* Crabeater Seal Elephant Seal Southern Elephant Seal Weddell Seal Northern fur seal |
op_relation |
https://dx.doi.org/10.1093/sysbio/syaa075 https://dx.doi.org/10.1111/j.1365-3113.1978.tb00120.x https://dx.doi.org/10.1093/nar/27.8.1767 https://dx.doi.org/10.1101/gr.083188.108 https://dx.doi.org/10.1093/gbe/evs088 https://dx.doi.org/10.1186/1756-3305-7-144 https://dx.doi.org/10.1093/gbe/evx007 https://dx.doi.org/10.1093/gbe/evt094 https://dx.doi.org/10.1186/1471-2164-15-751 https://dx.doi.org/10.1186/1471-2164-15-44 https://dx.doi.org/10.1016/j.ygeno.2020.09.005 https://dx.doi.org/10.1186/s12864-021-07859-w https://dx.doi.org/10.1186/s12864-015-1843-3 https://dx.doi.org/10.1111/syen.12350 https://dx.doi.org/10.1186/1741-7007-5-7 https://dx.doi.org/10.1007/s00300-015-1822-9 https://dx.doi.org/10.1007/s00436-014-4058-7 https://dx.doi.org/10.1126/science.8066445 https://dx.doi.org/10.1006/mpev.1997.0458 https://dx.doi.org/10.1080/10635159950127303 |
op_rights |
Creative Commons Attribution 4.0 International https://creativecommons.org/licenses/by/4.0/legalcode cc-by-4.0 |
op_doi |
https://doi.org/10.6084/m9.figshare.1956585910.1093/sysbio/syaa07510.1111/j.1365-3113.1978.tb00120.x10.1093/nar/27.8.176710.1101/gr.083188.10810.1093/gbe/evs08810.1186/1756-3305-7-14410.1093/gbe/evx00710.1093/gbe/evt09410.1186/1471-2164-15-75110.1186/1471 |
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