Submissions from 2020
Additional file 3 of Integrated Puncture Score: force–displacement weighted rind penetration tests improve stalk lodging resistance estimations in maize, Christopher J. Stubbs, Douglas D. Cook, Daniel J. Robertson, Christopher McMahan, and Will Seegmiller
Additional file 1 of Integrated Puncture Score: force–displacement weighted rind penetration tests improve stalk lodging resistance estimations in maize, Christopher J. Stubbs, Will Seegmiller, Douglas D. Cook, Christopher McMahan, and Daniel J. Robertson
The promise and the perils of resurveying to understand global change impacts, Katharine Stuble, Sharon Bewick, Arthur Shapiro, Susan Harrison, Mark Fisher, Matthew Forister, Andrew Latimer, and Laurel Fox
The effects of climate change on floral anthocyanin polymorphisms, Cierra Sullivan and Matthew Koski
Additional file 2 of AsHSP26.8a, a creeping bentgrass small heat shock protein integrates different signaling pathways to modulate plant abiotic stress response, Xinbo Sun, Liebao Han, Hong Luo, Zhigang Li, Junfei Zhu, and Xin Li
CCDC 1958147: Experimental Crystal Structure Determination, Maria I. Swasy, Kristopher G. Gross, Beau R. Brummel, William T. Pennington, Timothy R. Lex, Soham Panda, Lauren N. Giambalvo, Daniel C. Whitehead, Colin D. McMillen, and Khadijatul Kobra
A case of anti- pityriasis versicolor therapy that preserves healthy mycobiome, Jacek C. Szepietowski, Ewa Leniak, Sebastian Gnat, Lukasz Kozubowski, and Mariusz Dyląg
Data for the GMG Stokes paper, Clevenger T.C. and Heister Timo
Additional file 1 of Isolation and characterization of diverse microbial representatives from the human skin microbiome, Collin M. Timm, Thomas Mehoke, William Stone, David K. Karig, Matthew Pellicore, Bryan Brensinger, Seema Nayak, Curtisha Charles, Kristin Loomis, and Phillip P.A. Staniczenko
The deal.II tutorial step-50: Geometric Multigrid on adaptive meshes distributed in parallel, Heister Timo and C. Clevenger Thomas
dealii/candi: 9.2.0-r2, Heister Timo, Köcher Uwe, Rudolph Max, fvanmaele, Turcksin Bruno, Gassmoeller Rene, Corum Curt, WEI Xiaoyu, tcclevenger, Arndt Daniel, and Bangerth Wolfgang
Figure 10 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 15 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 17 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 18 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 19 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 1 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 21 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 25 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 29 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 30 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 32 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 33 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 34 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 37 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 38 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 39 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 3 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 5 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 6 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 7 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Figure 8 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Map 10 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Map 11 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Map 13 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Map 1 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Map 3 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Map 5 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Map 6 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Map 7 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Map 8 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Map 9 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Supplementary material 1 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino
Political System Attitudes Study - Pilot Wave, Stephen Utych, Matthew Rhodes-Purdy, Rachel Navarre, and Matthew Rhodes-Purdy
Identification and characterization of QTLs for fruit quality traits in peach through a multi-family approach, Eric Van De Weg, David H. Byrne, Silvia Carpenedo, Cassia Da Silva Linge, Zena J. Rawandoozi, Ksenija Gasic, Timothy P. Hartmann, and Lichun Cai
VidyaSamadi/WaccamawData: WaccamawData, Samadi Vidya
Combined Geotechnical and Geophysical Investigation of Texas Rivers Post Hurricane Harvey., Tech Virginia, Ravi Ravichandran, Nina Stark, University Clemson, Reem Jaber, Navid Jafari, and State University Louisiana
Disentangling interactions among mercury, immunity, and infection in a Neotropical bat community, Dmitriy Volokhov, Hannah Droke, Alexis Brown, Ticha Padgett-Stewart, Brock Fenton, Matthew Chumchal, Daniel Becker, Hugh Broders, Catherene Baijnauth, Thomas Rainwater, Nancy Simmons, Raina Plowright, Kelly Speer, and Jennifer Korstian
Data and supplemental tables from Colour dimorphism in labrid fishes as an adaptation to life on coral reefs, P.C. Wainwright, F. Santini, and J.R. Hodge
Data and supplemental tables from Colour dimorphism in labrid fishes as an adaptation to life on coral reefs, P.C. Wainwright, F. Santini, and J.R. Hodge
Divergent processes drive parallel evolution in marine and freshwater fishes, Peter Wainwright, Mike Collyer, Samantha Price, and Sarah Friedman
Additional file 2 of Prediction and prioritization of autism-associated long non-coding RNAs using gene expression and sequence features, Jun Wang and Liangjiang Wang
Additional file 3 of Prediction and prioritization of autism-associated long non-coding RNAs using gene expression and sequence features, Jun Wang and Liangjiang Wang
Prediction and prioritization of autism-associated long non-coding RNAs using gene expression and sequence features, Liangjiang Wang and Jun Wang
Supplemental Material for Brenton et al., 2020, Xiaoyun Wang, Erin L. Connolly, Zachary W. Brenton, Kathleen E. Jordan, Jeffrey C. Glaubitz, Matthew T. Myers, Brendon T. Juengst, Savanah M. Dale, Elizabeth A. Cooper, and Richard E. Boyles
Additional file 11 of Transcriptomic profiles of non-embryogenic and embryogenic callus cells in a highly regenerative upland cotton line (Gossypium hirsutum L.), Li Wen, John Lawson, Zhigang Li, Christopher A. Saski, Michael Smathers, Wei Li, Shuangxia Jin, Matthew West, Don Jones, and Stephen Parris
Additional file 5 of Transcriptomic profiles of non-embryogenic and embryogenic callus cells in a highly regenerative upland cotton line (Gossypium hirsutum L.), Li Wen, Michael Smathers, Don Jones, Stephen Parris, John Lawson, Zhigang Li, Shuangxia Jin, Matthew West, Wei Li, and Christopher A. Saski
CSD 1881440: Experimental Crystal Structure Determination, Yimei Wen, Tiffany M. Smith Pellizzeri, Rachel B. Getman, Steven Pellizzeri, Joseph W. Kolis, Colin D. McMillen, and George Chumanov
Additional file 9 of Transcriptomic profiles of non-embryogenic and embryogenic callus cells in a highly regenerative upland cotton line (Gossypium hirsutum L.), Matthew West, John Lawson, Michael Smathers, Stephen Parris, Li Wen, Don Jones, Christopher A. Saski, Wei Li, Shuangxia Jin, and Zhigang Li
Additional file 3 of Transcriptomic profiles of non-embryogenic and embryogenic callus cells in a highly regenerative upland cotton line (Gossypium hirsutum L.), Matthew West, Li Wen, Stephen Parris, Shuangxia Jin, Christopher A. Saski, John Lawson, Wei Li, Don Jones, Michael Smathers, and Zhigang Li
CCDC 1883834: Experimental Crystal Structure Determination, Modi Wetzler, Megan M. Sibley, Matthew S. Wasilewski, Alexandra M. North, Ian R. Ruohoniemi, and Colin D. Mcmillen
CCDC 1954260: Experimental Crystal Structure Determination, Daniel C. Whitehead, Joseph W. Kolis, Beau R. Brummel, Kinsey G. Lee, and Colin D. McMillen
CCDC 1954259: Experimental Crystal Structure Determination, Daniel C. Whitehead, Colin D. McMillen, Beau R. Brummel, Joseph W. Kolis, and Kinsey G. Lee
CCDC 1954262: Experimental Crystal Structure Determination, Daniel C. Whitehead, Colin D. McMillen, Beau R. Brummel, Kinsey G. Lee, and Joseph W. Kolis
CSD 1790459: Experimental Crystal Structure Determination, Daniel Willett, Garlea V. Ovidiu, Joseph W. Kolis, Michael A. McGuire, Tiffany M. Smith Pellizzeri, Liurukara D. Sanjeewa, Colin D. McMillen, and George Chumanov
Importance of Regional-Scale Auroral Precipitation and Electrical Field Variability to the Storm-Time Thermospheric Temperature Enhancement and Inversion Layer (TTEIL) in the Antarctic E Region, Haonan Wu and Xian Lu
Additional file 1 of The chromosome-level wintersweet (Chimonanthus praecox) genome provides insights into floral scent biosynthesis and flowering in winter, Zhongping Xu, Christopher A. Saski, Huihui Cheng, Lin Xiang, Jingpu Tian, Qiaomu Yan, Junzhong Shang, Kaige Zhao, Abbas Jamal, Longqing Chen, Xiuqun Liu, Shuangxia Jin, and Lai Li
The chromosome-level wintersweet (Chimonanthus praecox) genome provides insights into floral scent biosynthesis and flowering in winter, Zhongping Xu, Jingpu Tian, Huihui Cheng, Qiaomu Yan, Kaige Zhao, Abbas Jamal, Lai Li, Christopher A. Saski, Xiuqun Liu, Junzhong Shang, Shuangxia Jin, Longqing Chen, and Lin Xiang
CCDC 1987586: Experimental Crystal Structure Determination, Ashok Yadav, Dillip K. Panda, Sourav Saha, Shiyu Zhang, and Wei Zhou
Additional file 1 of Autonomous replication sequences from the Amaranthus palmeri eccDNA replicon enable replication in yeast, Allison Yaguchi, William T. Molin, Mark Blenner, and Christopher A. Saski
Additional file 2 of Autonomous replication sequences from the Amaranthus palmeri eccDNA replicon enable replication in yeast, Allison Yaguchi, William T. Molin, Mark Blenner, and Christopher A. Saski
Additional file 5 of Autonomous replication sequences from the Amaranthus palmeri eccDNA replicon enable replication in yeast, Allison Yaguchi, William T. Molin, Christopher A. Saski, and Mark Blenner
Additional file 5 of Autonomous replication sequences from the Amaranthus palmeri eccDNA replicon enable replication in yeast, Allison Yaguchi, Christopher A. Saski, William T. Molin, and Mark Blenner
Supplemental Material for Yanagawa et al., 2020, Aya Yanagawa, Coby Schal, Wen Huang, Trudy F.C. Mackay, Akihiko Yamamoto, and Ayako Wada-Katsumata
FIGURE 4. Ceraclea spp. n., female genitalia. 4A–4C in Interesting new Chinese species of Leptoceridae and Odontoceridae (Insecta: Trichoptera) from several recent collecting efforts, Lian-Fang Yang, Ben-Jin Hu, and John C. Morse
FIGURE 6 in Interesting new Chinese species of Leptoceridae and Odontoceridae (Insecta: Trichoptera) from several recent collecting efforts, Lian-Fang Yang, Ben-Jin Hu, and John C. Morse
FIGURE 7. Oecetis spp. n., female genitalia. 7A–7C in Interesting new Chinese species of Leptoceridae and Odontoceridae (Insecta: Trichoptera) from several recent collecting efforts, Lian-Fang Yang, Ben-Jin Hu, and John C. Morse
FIGURE 3 in Interesting new Chinese species of Leptoceridae and Odontoceridae (Insecta: Trichoptera) from several recent collecting efforts, Lian-Fang Yang, John C. Morse, and Ben-Jin Hu
Data from: Climate and soil nutrients differentially drive multidimensional fine root traits in ectomycorrhizal‐dominated alpine coniferous forests, Huajun Yin, JunXiang Ding, Ziliang Zhang, Qing Liu, Deliang Kong, Qin Cai, and Juan Xiao
CSD 2006494: Experimental Crystal Structure Determination, Eric Zhang, Shani Egodawatte, Navindra Keerthisinghe, Mark D. Smith, Vladislav V. Klepov, Hans-Conrad zur Loye, and Stephen H. Foulger
CSD 2006491: Experimental Crystal Structure Determination, Eric Zhang, Mark D. Smith, Navindra Keerthisinghe, Hans-Conrad zur Loye, Vladislav V. Klepov, Stephen H. Foulger, and Shani Egodawatte
The role of surgery type in postoperative atrial fibrillation and in-hospital mortality in esophageal cancer patients with preserved left ventricular ejection fraction, Lu Zhang, Chenyang Jiang, Laite Chen, Guosheng Fu, and Lu Shi
Tectono-magmatic events of the Qilian orogenic belt in northern Tibet: new insights from detrital zircon geochronology of river sands, Shuo Zhang, Ling Fu, Alex Pullen, Wei Zhang, Xing Jian, Dongming Hong, and Hanghai Liang
Effect of soil carbon amendments in reversing the legacy effect of plant invasion, Ziliang Zhang, Prasanta Bhowmik, and Vidya Suseela
Effect of soil carbon amendments in reversing the legacy effect of plant invasion, Ziliang Zhang, Vidya Suseela, and Prasanta Bhowmik
CCDC 1987585: Experimental Crystal Structure Determination, Wei Zhou, Ashok Yadav, Shiyu Zhang, Dillip K. Panda, and Sourav Saha
Additional file 2 of AsHSP26.8a, a creeping bentgrass small heat shock protein integrates different signaling pathways to modulate plant abiotic stress response, Junfei Zhu, Hong Luo, Xin Li, Zhigang Li, Xinbo Sun, and Liebao Han
Submissions from 2019
The Ambidextrous Sales Force: Aligning Salesperson Polychronicity and Selling Contexts for Sales-Service Behaviors and Customer Value, Raj Agnihotri, Zachary Hall, and Ryan Mullins
Forecasting the Prevalence of Diabetes Mellitus Using Econometric Models, Zhanay Akanov, Amy Apon, Sanjay Kalra, Nurbek Saparkhojayev, and Assel Mukasheva
Data from: Genetic analyses in Lake Malawi cichlids identify new roles for Fgf signaling in scale shape variation, R. Craig Albertson, Kenta C. Kawasaki, Kara E. Powder, and Emily R. Tetrault
Data from: Genetic analyses in Lake Malawi cichlids identify new roles for Fgf signaling in scale shape variation, R. Craig Albertson, Kenta C. Kawasaki, Emily R. Tetrault, and Kara E. Powder
Data from: White shark genome reveals ancient elasmobranch adaptations associated with wound healing and the maintenance of genome stability, Agostinho Antunes, Nicholas J. Marra, Minghui Wang, Chuck Winkler, Michael J. Stanhope, Salvador Jorgensen, Stephen J. O’Brien, Paulina Pavinski Bitar, Bryce J. Stanhope, Qi Sun, Mike Rayko, Aleksey Komissarov, Sergey Kliver, Mahmood S. Shivji, Vincent P. Richards, and Nathaniel K. Jue
Perceived supports and evidence-based teaching in college STEM, Oriana R. Aragón, Andrew J. Cavanagh, Jennifer Frederick, Meghan E. Bathgate, Jonathan K. Waterhouse, and Mark J. Graham
DATASET: De novo assembly and functional annotation of the heart + hemolymph transcriptome in the Caribbean spiny lobster Panulirus argus, J. Antonio Baeza and Matthew D MacManes
Figure 4 in An integrative taxonomic and phylogenetic approach reveals a complex of cryptic species in the 'peppermint' shrimp Lysmata wurdemanni sensu stricto, J. Antonio Baeza and Sanjeevi Prakash
The complete mitochondrial genome and description of a new cryptic species of Benedenia Diesing, 1858 (Monogenea: Capsalidae), a major pathogen infecting the yellowtail kingfish Seriola lalandi Valenciennes in the South-East Pacific, J. Antonio Baeza, Fabiola A. Sepúlveda, and M. Teresa González
Replication Materials for Barkowski/McLaughlin JHR 2020, Scott Barkowski and Joanne Song McLaughlin
raw data for version 2 of article " Effect of environmental and cultural conditions on medium pH and explant growth performance of Douglas-fir", Rick Bates, Chien-Chih Chen, and John Carlson
MOESM3 of Alu insertion polymorphisms shared by Papio baboons and Theropithecus gelada reveal an intertwined common ancestry, Mark A. Batzer, Jessica M. Storer, Paulina Gonzalez-Quiroga, Jeffrey Rogers, Lydia C. Rewerts, Corey P. St. Romain, Jerilyn A. Walker, Vallmer E. Jordan, Thomas O. Beckstrom, Catherine E. Rockwell, Miriam K. Konkel, Cody J. Steely, and Clifford J. Jolly
SystemsGenetics/ACE: Version 3.2.0, Shealy Ben, Smith Melissa, B Josh, Feltus Alex, and Ficklin Stephen