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Genome Sequences of Marine Shrimp Exopalaemon carinicauda Holthuis Provide Insights into Genome Size Evolution of Caridea

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471250953.bi0410s25openalex-snapshot

Using RepeatMasker to Identify Repetitive Elements in Genomic Sequences

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Numt, a recent transfer and tandem amplification of mitochondrial DNA to the nuclear genome of the domestic cat

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The first genome size estimates for six species of krill (Malacostraca, Euphausiidae): large genomes at the north and south poles

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DIRS retroelements in arthropods: identification of the recently active TcDirs1 element in the red flour beetle Tribolium castaneum

inferredcites →https://doi.org/10.1007/s13131-013-0261-0openalex-snapshot

Enhanced resistance of marine shrimp Exopalamon carincauda Holthuis to WSSV by injecting live VP28-recombinant bacteria

inferredcites →https://doi.org/10.1016/0044-8486(91)90325-2openalex-snapshot

Karyological studies on the freshwater prawn Macrobrachium rosenbergii

inferredcites →https://doi.org/10.1016/j.fsi.2012.10.026openalex-snapshot

Immune gene discovery by expressed sequence tag (EST) analysis of hemocytes in the ridgetail white prawn Exopalaemon carinicauda

inferredcites →https://doi.org/10.1016/j.gene.2009.02.014openalex-snapshot

The complete mitochondrial genome of the ridgetail white prawn Exopalaemon carinicauda Holthuis, 1950 (Crustacean: Decapoda: Palaemonidae) revealed a novel rearrangement of tRNA genes

inferredcites →https://doi.org/10.1023/a:1016072014259openalex-snapshot

Transposable elements and the evolution of genome size in eukaryotes

inferredcites →https://doi.org/10.1038/33577openalex-snapshot

Gene translocation links insects and crustaceans

inferredcites →https://doi.org/10.1038/hdy.2008.80openalex-snapshot

Genome size evolution: Within-species variation in genome size

inferredcites →https://doi.org/10.1038/hdy.2015.89openalex-snapshot

Ancestral whole-genome duplication in the marine chelicerate horseshoe crabs

inferredcites →https://doi.org/10.1038/nature08696openalex-snapshot

The sequence and de novo assembly of the giant panda genome

inferredcites →https://doi.org/10.1038/nature11413openalex-snapshot

The oyster genome reveals stress adaptation and complexity of shell formation

inferredcites →https://doi.org/10.1038/ncomms4657openalex-snapshot

The rainbow trout genome provides novel insights into evolution after whole-genome duplication in vertebrates

inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot

Fast gapped-read alignment with Bowtie 2

inferredcites →https://doi.org/10.1038/nprot.2013.084openalex-snapshot

De novo transcript sequence reconstruction from RNA-Seq: reference generation and analysis with Trinity

inferredcites →https://doi.org/10.1038/srep15612openalex-snapshot

Genome survey and high-density genetic map construction provide genomic and genetic resources for the Pacific White Shrimp Litopenaeus vannamei

inferredcites →https://doi.org/10.1038/srep17464openalex-snapshot

Phylogenetics reveals the crustacean order Amphionidacea to be larval shrimps (Decapoda: Caridea)

inferredcites →https://doi.org/10.1073/pnas.0811575106openalex-snapshot

The frequency of polyploid speciation in vascular plants

inferredcites →https://doi.org/10.1073/pnas.0901282106openalex-snapshot

Characterization and distribution of retrotransposons and simple sequence repeats in the bovine genome

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The impact of long-distance horizontal gene transfer on prokaryotic genome size

inferredcites →https://doi.org/10.1080/10635150390235520openalex-snapshot

A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood

inferredcites →https://doi.org/10.1093/aob/mci008openalex-snapshot

Mechanisms of Recent Genome Size Variation in Flowering Plants

inferredcites →https://doi.org/10.1093/bioinformatics/btg034openalex-snapshot

TIGR Gene Indices clustering tools (TGICL): a software system for fast clustering of large EST datasets

inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot

MrBayes 3: Bayesian phylogenetic inference under mixed models

inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot

Fast and accurate short read alignment with Burrows–Wheeler transform

inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot

The Sequence Alignment/Map format and SAMtools

inferredcites →https://doi.org/10.1093/bioinformatics/btp698openalex-snapshot

Fast and accurate long-read alignment with Burrows–Wheeler transform

inferredcites →https://doi.org/10.1093/bioinformatics/btr011openalex-snapshot

A fast, lock-free approach for efficient parallel counting of occurrences of k -mers

inferredcites →https://doi.org/10.1093/bioinformatics/btv351openalex-snapshot

BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs

inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot

MUSCLE: multiple sequence alignment with high accuracy and high throughput

inferredcites →https://doi.org/10.1093/nar/gkj118openalex-snapshot

TreeFam: a curated database of phylogenetic trees of animal gene families

inferredcites →https://doi.org/10.1093/nar/gkt1055openalex-snapshot

TreeFam v9: a new website, more species and orthology-on-the-fly

inferredcites →https://doi.org/10.1098/rstb.2014.0331openalex-snapshot

What's in a genome? The C-value enigma and the evolution of eukaryotic genome content

inferredcites →https://doi.org/10.1101/gr.229202openalex-snapshot

BLAT —The BLAST -Like Alignment Tool

inferredcites →https://doi.org/10.1101/gr.5290206openalex-snapshot

Doubling genome size without polyploidization: Dynamics of retrotransposition-driven genomic expansions in Oryza australiensis , a wild relative of rice

inferredcites →https://doi.org/10.1105/tpc.021345openalex-snapshot

Widespread Paleopolyploidy in Model Plant Species Inferred from Age Distributions of Duplicate Genes[W]

inferredcites →https://doi.org/10.1111/1462-2920.12883openalex-snapshot

Genome analyses suggest the presence of polyploidy and recent human‐driven expansions in eight global populations of the honeybee pathogen N osema ceranae

inferredcites →https://doi.org/10.1111/j.1463-6409.2009.00410.xopenalex-snapshot

Phylogenetic position, systematic status, and divergence time of the Procarididea (Crustacea: Decapoda)

inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01293.xopenalex-snapshot

Duplication and DNA segmental loss in the rice genome: implications for diploidization

inferredcites →https://doi.org/10.11113/mjfas.v10n2.57openalex-snapshot

Pitfalls of ascertainment biases in genome annotations—computing comparable protein domain distributions in eukarya

inferredcites →https://doi.org/10.1117/1.jmi.1.1.014005openalex-snapshot

Impact of family structure and common environment on heritability estimation for neuroimaging genetics studies using Sequential Oligogenic Linkage Analysis Routines

inferredcites →https://doi.org/10.1126/science.1197761openalex-snapshot

The Ecoresponsive Genome of Daphnia pulex

inferredcites →https://doi.org/10.1128/aem.02194-08openalex-snapshot

Oenococcus oeni Genome Plasticity Is Associated with Fitness

inferredcites →https://doi.org/10.1139/g07-108openalex-snapshot

Large genomes among caridean shrimp

inferredcites →https://doi.org/10.1139/g09-027openalex-snapshot

Survey of genome size in 28 hydrothermal vent species covering 10 families

inferredcites →https://doi.org/10.1139/gen-2015-0206openalex-snapshot

Patterns of genome size variation in snapping shrimp

inferredcites →https://doi.org/10.1146/annurev.genet.33.1.479openalex-snapshot

Plant Retrotransposons

inferredcites →https://doi.org/10.1146/annurev.genom.8.080706.092416openalex-snapshot

Repetitive Sequences in Complex Genomes: Structure and Evolution

inferredcites →https://doi.org/10.1186/1471-2148-11-356openalex-snapshot

Pathogen-origin horizontally transferred genes contribute to the evolution of Lepidopteran insects

inferredcites →https://doi.org/10.1186/1471-2148-13-165openalex-snapshot

Horizontally transferred genes in the genome of Pacific white shrimp, Litopenaeus vannamei

inferredcites →https://doi.org/10.1186/1471-2164-12-248openalex-snapshot

Horizontal gene transfer in silkworm, Bombyx mori

inferredcites →https://doi.org/10.1186/1471-2164-13-631openalex-snapshot

Evolution and phylogeny of the mud shrimps (Crustacea: Decapoda) revealed from complete mitochondrial genomes

inferredcites →https://doi.org/10.1186/1471-2164-14-447openalex-snapshot

Exceptionally high cumulative percentage of NUMTs originating from linear mitochondrial DNA molecules in the Hydra magnipapillata genome

inferredcites →https://doi.org/10.1186/1471-2164-14-604openalex-snapshot

L_RNA_scaffolder: scaffolding genomes with transcripts

inferredcites →https://doi.org/10.1186/1471-2180-12-77openalex-snapshot

Comparative transcriptomic analysis of streptococcus pseudopneumoniae with viridans group streptococci

inferredcites →https://doi.org/10.1186/1745-6150-4-28openalex-snapshot

On the need for widespread horizontal gene transfers under genome size constraint

inferredcites →https://doi.org/10.1186/2047-217x-1-18openalex-snapshot

SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler

inferredcites →https://doi.org/10.1186/2047-217x-3-9openalex-snapshot

Joint assembly and genetic mapping of the Atlantic horseshoe crab genome reveals ancient whole genome duplication

inferredcites →https://doi.org/10.1186/s12862-015-0339-8openalex-snapshot

Do larger genomes contain more diverse transposable elements?

inferredcites →https://doi.org/10.1186/s13742-016-0112-yopenalex-snapshot

Draft genome of the Chinese mitten crab, Eriocheir sinensis

inferredcites →https://doi.org/10.1371/journal.pgen.1000827openalex-snapshot

Bacterial Genes in the Aphid Genome: Absence of Functional Gene Transfer from Buchnera to Its Host

inferredcites →https://doi.org/10.1371/journal.pone.0030619openalex-snapshot

NGS QC Toolkit: A Toolkit for Quality Control of Next Generation Sequencing Data

inferredcites →https://doi.org/10.1534/g3.116.034082openalex-snapshot

CRISPR/Cas9-Mediated Genome Editing and Mutagenesis of EcChi4 in Exopalaemon carinicauda

inferredcites →https://doi.org/10.2307/1548667openalex-snapshot

Meiotic Chromosome Complements and Nuclear DNA Contents of Four Species of Shrimps of the Genus Penaeus

inferredcites →https://doi.org/10.3390/md12031419openalex-snapshot

Genomic Sequence and Experimental Tractability of a New Decapod Shrimp Model, Neocaridina denticulata

inferredcites →https://doi.org/10.3897/asp.67.e31691openalex-snapshot

The Decapod Tree of Life: Compiling the Data and Moving toward a Consensus of Decapod Evolution

inferredcites →https://doi.org/10.4238/2015.october.9.20openalex-snapshot

Analysis of ITS1 sequences and genetic relationships between populations of ridgetail white prawn, Exopalaemon carinicauda, in the East China Sea

inferredcites →https://doi.org/10.7554/elife.20062openalex-snapshot

The genome of the crustacean Parhyale hawaiensis, a model for animal development, regeneration, immunity and lignocellulose digestion

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/jez.b.23118openalex-snapshot

Identification of Hox genes and their expression profiles during embryonic development of the emerging model organism, Macrobrachium olfersii

inferred← citeshttps://doi.org/10.1007/978-1-0716-4322-8_6openalex-snapshot

Exploring Hox Genes and Their Temporal Expression in an Embryonic Model of Freshwater Crustaceans

inferred← citeshttps://doi.org/10.1007/s00441-020-03223-8openalex-snapshot

Ovarian development pattern and vitellogenesis of ridgetail white prawn, Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1007/s10499-021-00747-wopenalex-snapshot

Genomic selection in salmonids: new discoveries and future perspectives

inferred← citeshttps://doi.org/10.1007/s11756-026-02330-1openalex-snapshot

Mapping global research trends in Palaemon and related palaemonid shrimps: a scientometric analysis

inferred← citeshttps://doi.org/10.1007/s12038-018-9741-xopenalex-snapshot

Investigating the genetic and epigenetic basis of big biological questions with the parthenogenetic marbled crayfish: A review and perspectives

inferred← citeshttps://doi.org/10.1007/s13205-024-04121-4openalex-snapshot

Genome sequencing of Caridina pseudogracilirostris and its comparative analysis with malacostracan crustaceans

inferred← citeshttps://doi.org/10.1007/s13258-019-00787-wopenalex-snapshot

Molt-dependent transcriptome analysis of claw muscles in Chinese mitten crab Eriocheir sinensis

inferred← citeshttps://doi.org/10.1016/j.aqrep.2022.101366openalex-snapshot

Construction of a cytidine base editor based on Exopalaemon carinicauda cytidine deaminase and its application in crustacean genome editing

inferred← citeshttps://doi.org/10.1016/j.aquaculture.2020.735357openalex-snapshot

Research advances in the genomics and applications for molecular breeding of aquaculture animals

inferred← citeshttps://doi.org/10.1016/j.cbpb.2025.111093openalex-snapshot

Changes in the biochemical and gene expression profiles of Palaemon carinicauda during ovarian development

inferred← citeshttps://doi.org/10.1016/j.fsi.2017.09.065openalex-snapshot

A CRISPR/Cas9-mediated mutation in chitinase changes immune response to bacteria in Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1016/j.fsi.2018.02.004openalex-snapshot

Immune function against bacteria of chitin deacetylase 1 (EcCDA1) from Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1016/j.fsi.2018.04.002openalex-snapshot

CRISPR/Cas9-mediated deletion of EcMIH shortens metamorphosis time from mysis larva to postlarva of Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1016/j.fsi.2018.08.046openalex-snapshot

Biological function of a gC1qR homolog (EcgC1qR) of Exopalaemon carinicauda in defending bacteria challenge

inferred← citeshttps://doi.org/10.1016/j.fsi.2019.07.046openalex-snapshot

Cloning of a trehalose-6-phosphate synthase gene from Exopalaemon carinicauda and its expression response to bacteria challenge

inferred← citeshttps://doi.org/10.1016/j.fsi.2019.12.037openalex-snapshot

CRISPR/Cas9-mediated deletion of one carotenoid isomerooxygenase gene (EcNinaB-X1) from Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1016/j.fsi.2020.12.009openalex-snapshot

Genomic structure, expression and functional characterization of arginine kinase (EcAK) from Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1016/j.fsi.2022.06.003openalex-snapshot

A novel type I Crustin from Exopalaemon carinicauda: Antimicrobial ability related to conserved cysteine

inferred← citeshttps://doi.org/10.1016/j.gene.2018.01.046openalex-snapshot

Molecular characterization and function of β-N-acetylglucosaminidase from ridgetail white prawn Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.02.073openalex-snapshot

CRISPR/Cas9-mediated deletion of β, β-carotene 9′, 10′-oxygenase gene (EcBCO2) from Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.152499openalex-snapshot

Three-dimensional chromatin architecture in crustaceans: Emerging evidence, structural principles, and future directions: A review

inferred← citeshttps://doi.org/10.1016/j.margen.2017.12.006openalex-snapshot

Genomic resources and comparative analyses of two economical penaeid shrimp species, Marsupenaeus japonicus and Penaeus monodon

inferred← citeshttps://doi.org/10.1016/j.margen.2020.100751openalex-snapshot

Improved genomic resources for the black tiger prawn (Penaeus monodon)

inferred← citeshttps://doi.org/10.1016/j.marpolbul.2022.113324openalex-snapshot

Metallothionein-1 gene from Exopalaemon carinicauda and its response to heavy metal ions challenge

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.170415openalex-snapshot

The effect of astaxanthin on the alkalinity stress resistance of Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.175358openalex-snapshot

Positive selection in cilia-related genes may facilitate deep-sea adaptation of Thermocollonia jamsteci

inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.07.001openalex-snapshot

CRISPR/Cas9-mediated mutation reveals Pax6 is essential for development of the compound eye in Decapoda Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1016/j.ygcen.2020.113528openalex-snapshot

Gonadulins, the fourth type of Insulin-related peptides in Decapods

inferred← citeshttps://doi.org/10.1017/s0025315423000504openalex-snapshot

A first genome survey sequencing of alvinocaridid shrimp Shinkaicaris leurokolos in deep-sea hydrothermal vent environment

inferred← citeshttps://doi.org/10.1038/s41597-024-03423-9openalex-snapshot

Chromosome-level genome assembly of ridgetail white shrimp Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1038/s41598-019-47509-6openalex-snapshot

Production of WW males lacking the masculine Z chromosome and mining the Macrobrachium rosenbergii genome for sex-chromosomes

inferred← citeshttps://doi.org/10.1038/s41598-019-52656-xopenalex-snapshot

The gene structure and hypervariability of the complete Penaeus monodon Dscam gene

inferred← citeshttps://doi.org/10.1038/s42003-021-01921-9openalex-snapshot

Lineage-level divergence of copepod glycerol transporters and the emergence of isoform-specific trafficking regulation

inferred← citeshttps://doi.org/10.1073/pnas.2216574120openalex-snapshot

Scavenger receptor B2, a type III membrane pattern recognition receptor, senses LPS and activates the IMD pathway in crustaceans

inferred← citeshttps://doi.org/10.1093/gigascience/giaa160openalex-snapshot

A chromosome-level genome assembly of the oriental river prawn, Macrobrachium nipponense

inferred← citeshttps://doi.org/10.1093/jcbiol/ruz074openalex-snapshot

Genome survey and identification of polymorphic microsatellites provide genomic information and molecular markers for the red crab Charybdis feriatus (Linnaeus, 1758) (Decapoda: Brachyura: Portunidae)

inferred← citeshttps://doi.org/10.1111/1755-0998.13357openalex-snapshot

A chromosome‐level assembly of the black tiger shrimp ( Penaeus monodon ) genome facilitates the identification of growth‐associated genes

inferred← citeshttps://doi.org/10.1111/1755-0998.13667openalex-snapshot

Do pseudogenes pose a problem for metabarcoding marine animal communities?

inferred← citeshttps://doi.org/10.1111/jwas.12650openalex-snapshot

Characteristic analysis of simple sequence repeats in the ridgetail white prawn Exopalaemon carinicauda genome and its application in parentage assignment

inferred← citeshttps://doi.org/10.1111/raq.12791openalex-snapshot

Recent advances in crustacean genomics and their potential application in aquaculture

inferred← citeshttps://doi.org/10.1155/2020/5735968openalex-snapshot

Effects of Inbreeding on Genetic Characteristic, Growth, Survival Rates, and Immune Responses of a New Inbred Line of Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.1163/15685403-00003930openalex-snapshot

Crustacean vitellogenin: a systematic and experimental analysis of their genes, genomes, mRNAs and proteins; and perspective to Next Generation Sequencing

inferred← citeshttps://doi.org/10.1186/s12864-019-5981-xopenalex-snapshot

Genome survey and high-resolution backcross genetic linkage map construction of the ridgetail white prawn Exopalaemon carinicauda applications to QTL mapping of growth traits

inferred← citeshttps://doi.org/10.1186/s12864-024-10453-5openalex-snapshot

Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.21203/rs.2.9774/v1openalex-snapshot

The gene structure and super-hypervariability of the complete Penaeus monodon Dscam gene

inferred← citeshttps://doi.org/10.21203/rs.3.rs-3930896/v1openalex-snapshot

Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.3389/fendo.2022.986491openalex-snapshot

CRISPR/Cas9-mediated mutation on an insulin-like peptide encoding gene affects the growth of the ridgetail white prawn Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.3389/fendo.2023.1266641openalex-snapshot

CRISPR/Cas9-mediated gene mutation of EcIAG leads to sex reversal in the male ridgetail white prawn Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.3389/fgene.2018.00693openalex-snapshot

Genomic Selection in Aquaculture: Application, Limitations and Opportunities With Special Reference to Marine Shrimp and Pearl Oysters

inferred← citeshttps://doi.org/10.3389/fgene.2019.00298openalex-snapshot

High-Density Genetic Linkage Maps Provide Novel Insights Into ZW/ZZ Sex Determination System and Growth Performance in Mud Crab (Scylla paramamosain)

inferred← citeshttps://doi.org/10.3389/fmars.2022.906730openalex-snapshot

Full-Length Transcriptome Sequencing and Comparative Transcriptomic Analysis Provide Insights Into the Ovarian Maturation of Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.3389/fmars.2022.995790openalex-snapshot

Comparative transcriptomic analysis and validation of the ovary and testis in the ridgetail white prawn (Exopalaemon carinicauda)

inferred← citeshttps://doi.org/10.3389/fmars.2023.1278131openalex-snapshot

De novo genome and transcriptome assembly of Kelletia kelletii, a coastal gastropod and fisheries species exhibiting a northern range expansion

inferred← citeshttps://doi.org/10.3390/genes12030401openalex-snapshot

A Survey of Transposon Landscapes in the Putative Ancient Asexual Ostracod Darwinula stevensoni

inferred← citeshttps://doi.org/10.3390/ijms21072599openalex-snapshot

Molecular Cytogenetic Analysis in Freshwater Prawns of the Genus Macrobrachium (Crustacea: Decapoda: Palaemonidae)

inferred← citeshttps://doi.org/10.3390/ijms25021089openalex-snapshot

Genome-Wide Identification of Vitellogenin Gene Family and Comparative Analysis of Their Involvement in Ovarian Maturation in Exopalaemon carinicauda

inferred← citeshttps://doi.org/10.3390/ijms26041605openalex-snapshot

Effects of Alexandrium pacificum Exposure on Exopalaemon carinicauda: Hepatopancreas Histology, Antioxidant Enzyme Activity, and Transcriptome Analysis

inferred← citeshttps://doi.org/10.3390/ijms27021056openalex-snapshot

Multi-Omics Profiling of the Hepatopancreas of Ridgetail White Prawn Exopalaemon carinicauda Under Sulfate Stress

inferred← citeshttps://doi.org/10.6084/m9.figshare.25989173openalex-snapshot

Additional file 1 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.25989303openalex-snapshot

Additional file 2 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730322openalex-snapshot

Additional file 3 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730325openalex-snapshot

Additional file 4 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730328openalex-snapshot

Additional file 5 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730331openalex-snapshot

Additional file 6 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730334openalex-snapshot

Additional file 7 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730337openalex-snapshot

Additional file 8 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730340openalex-snapshot

Additional file 9 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730343openalex-snapshot

Additional file 10 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730346openalex-snapshot

Additional file 11 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730349openalex-snapshot

Additional file 12 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

inferred← citeshttps://doi.org/10.6084/m9.figshare.26730352openalex-snapshot

Additional file 13 of Comparative transcriptomic analysis primarily explores the molecular mechanism of compound eye formation in Neocaridina denticulata sinensis

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