| name | bio-genome-annotation-repeat-annotation |
| description | Discovers, classifies, and masks repetitive elements and transposable elements with RepeatModeler2 (de novo family library), RepeatMasker (masking against a library), EDTA (plant/structural TEs), or EarlGrey (auto-curating wrapper), and quantifies TE expression from RNA-seq with TEtranscripts/SQuIRE. Covers de-novo-library-as-curation-project, soft-vs-hard masking, the domesticated-gene over-masking massacre, Dfam-vs-RepBase, TE classification (Class I/II, family-vs-copy), Kimura repeat landscapes, LAI, and the RNA-seq multimapping problem. Use when masking repeats before gene prediction, building a TE library for a non-model genome, or analyzing transposable-element content or expression. |
| origin | openai4s |
| category | bioskills/genome-annotation |
| metadata | {"tool_type":"cli","primary_tool":"RepeatMasker","third_party":{"name":"GPTomics/bioSkills","repository":"https://github.com/GPTomics/bioSkills","commit":"d91ed3d563019e649dc854c56ccd62551359488a","license":"MIT"}} |
Version Compatibility
Reference examples tested with: RepeatModeler 2.0.5+, RepeatMasker 4.1.5+, EDTA 2.1+, EarlGrey 4.0+, TEtranscripts 2.2+, matplotlib 3.8+, pandas 2.2+.
Before using code patterns, verify installed versions match. If versions differ:
- CLI:
<tool> --version then <tool> --help to confirm flags
- Python:
pip show <package> then help(module.function) to check signatures
The library database version matters as much as the binary: RepeatMasker now ships with Dfam (open); RepBase has been paywalled since May 2019, so any pipeline that "requires RepBase" is a reproducibility/access hazard - record the Dfam release and library provenance. If code throws an error, introspect the installed tool and adapt rather than retrying.
Repeat and Transposable Element Annotation
"Mask repeats in my genome assembly" -> Build a de novo repeat-family library, annotate copies genome-wide, and soft-mask them as a prerequisite for gene prediction.
- CLI:
RepeatModeler -database mydb -LTRStruct (library), RepeatMasker -lib lib.fa -xsmall assembly.fa (soft-mask), or EarlGrey/EDTA.pl (wrappers)
The Single Most Important Modern Insight -- The Library Is the Experiment, and the Assembly Caps It
Two load-bearing truths the masker hides:
-
De novo library construction is a curation research project, not a button. A RepeatModeler2 run emits mydb-families.fa overnight - a draft of a draft: consensi are routinely 5'-truncated (L1 looks 1.5 kb when the active element is 6 kb), boundary-bled into flanking unique sequence, chimeric (two families merged), and 30-60% "Unknown" on a non-model genome. The dominant error in published TE annotations is the library, not the masker engine. Crucially, masking percentage is robust to a bad library (a chimeric consensus still masks roughly the right real estate), so the headline number survives while everything downstream rots: inflated family counts, wrong classification, distorted age landscapes, and - the killer - host-gene-contaminated consensi that silently mask real genes. Masking + gross % can use an automated library; any per-family biological claim (this family is young/active/novel) needs curation (Goubert 2022 Mob DNA 13:7; TE-Aid; MCHelper).
-
Annotation quality is capped by assembly quality. Short-read de Bruijn assemblers collapse near-identical TE copies and drop the youngest (most identical, most biologically active) ones, so short-read assemblies systematically under-count TEs and bias the age distribution toward "old" - which masquerades as the real signal "this lineage has no recent activity." Software cannot recover what the assembler threw away. Always ask what assembly a "% repeat" came from; HiFi/T2T raised the ceiling (LAI measures it) but T2T satellite/centromere repeats still exceed what the standard TE toolchain can annotate.
Tool Taxonomy
| Tool | Citation | Role | When |
|---|
| RepeatModeler2 | Flynn 2020 PNAS | de novo family discovery -> consensus library | discover genome-specific families (run -LTRStruct) |
| RepeatMasker | Smit/Hubley/Green (software) | annotate/mask a genome against a library | the masking step; does not discover families |
| EarlGrey | Baril 2024 MBE | wraps RepeatModeler2 + auto consensus-elongation + RepeatMasker + plots | non-model default; minimal hand-work |
| EDTA | Ou 2019 Genome Biol | structural LTR/TIR/Helitron discovery + filtering | plant / structurally-rich genomes |
| LTR_retriever | Ou & Jiang 2018 Plant Physiol | isolate intact LTR-RTs; feeds LAI | LTR focus / assembly-quality (LAI) |
| TRF | Benson 1999 NAR | tandem/satellite repeats | a different algorithm class from TE maskers |
| RepeatClassifier / DeepTE / TERL | Flynn 2020; Yan 2020 | classify unknown consensi | attack the "Unknown" fraction (validate; can mislabel) |
Dfam (open) vs RepBase (paywalled since 2019) is the database schism - modern open pipelines build on Dfam + de novo. Engine -e: rmblast (default, consensus FASTA) vs nhmmer (Dfam profile HMMs, more sensitive for ancient repeats, slower) - the same genome reads a higher % with HMM detection.
Decision Tree by Scenario
| Scenario | Recommended | Why |
|---|
| Non-model eukaryote, defensible answer, minimal hand-work | EarlGrey | RepeatModeler2 + auto-curation + clean outputs |
| Plant / structurally-rich TE genome | EDTA | best-in-class LTR/TIR/Helitron structural annotation + host-gene filtering |
| Well-covered vertebrate, just need masking | RepeatMasker -species against Dfam | curated families already exist |
| Mask before gene prediction | RepeatMasker -xsmall (soft) + decontaminated library | predictors need soft-masking |
| Publication-grade TE biology claim | de novo -> manual curation (Goubert protocol, TE-Aid) | automated library is the start, not the end |
| Tandem/satellite/centromeric repeats | TRF + satellite tools (not RepeatMasker) | library-based TE tools don't see tandem arrays |
| TE expression from RNA-seq | -> TEtranscripts/SQuIRE (EM multimapper handling) | see expression section |
| TE insertion polymorphisms from reads | -> variant-calling (MELT/TEPID) | out of scope here |
RepeatModeler2 -> RepeatMasker (the canonical pair)
BuildDatabase -name mydb assembly.fa
RepeatModeler -database mydb -threads 16 -LTRStruct
RepeatMasker -lib mydb-families.fa -xsmall -gff -e rmblast -pa 16 -dir rm_out assembly.fa
-xsmall = soft-mask (lowercase) - the key flag, the one people get wrong. Default .masked output hard-masks with N; -x masks with X. -nolow skips low-complexity/simple repeats (often wanted before gene prediction - see below). Outputs: .masked, .out, .tbl (summary %), .align (needed for the landscape).
Soft vs Hard Masking (Critical, and the Over-Masking Massacre)
- Gene prediction needs SOFT-masking. Modern predictors (AUGUSTUS/GeneMark/BRAKER) avoid nucleating models in lowercase but let exons extend into repeats - real genes have TE-derived exons and TE-filled introns. Hard-masking (N) destroys sequence: any gene overlapping a repeat is truncated or never called, and the predictor reports nothing - no error, no log. The gene is simply absent.
- Over-aggressive soft-masking is also a failure. A gene whose promoter sits in an LTR, or a young gene inside a recent TE burst, gets suppressed because the predictor won't start a model in a heavily-lowercased locus. Before gene prediction, soft-mask interspersed repeats only and skip low-complexity (
-nolow) - simple repeats overlap real coding microsatellites and low-complexity protein domains.
- The domesticated-gene massacre. A de novo library contains fragments of real multicopy gene families because they look repetitive - and masking them deletes the genome's most interesting genes. Named casualties: RAG1/RAG2 (domesticated Transib transposase; V(D)J recombination), syncytins (captured retroviral env; placentation), SETMAR/Metnase (Hsmar1 mariner + SET domain; DNA repair), CENP-B (pogo transposase; centromere), and the KRAB-ZNF arrays (~350+ primate zinc-finger genes that exist to repress TEs - masking them deletes the genome's anti-TE machinery). Defense: decontaminate the library against a protein DB before masking (EDTA does a version; RepeatModeler2 does not by default). Treat any gene model falling entirely inside a masked "TE" as a flag to investigate, not a finished call.
TE Classification (Wicker-compatible)
- Class I (retrotransposons, copy-and-paste via RNA + RT): LTR-RTs (Ty3/Gypsy, Ty1/Copia - dominate large plant genomes), LINEs (autonomous, often 5'-truncated), SINEs (non-autonomous, e.g. Alu).
- Class II (DNA transposons, mostly cut-and-paste): TIR superfamilies (hAT, Tc1/Mariner, CACTA, PIF/Harbinger, Mutator), Helitrons (rolling-circle, can capture host genes), MITEs (non-autonomous TIR derivatives, EDTA reclassifies ≤600 bp).
- Family vs copy: a family is one consensus in the library (~thousands); a copy/insertion is one genomic locus matching it (millions). "% genome masked" counts copies; classification is family-level; "10,000 TEs" is ambiguous between the two.
- Full-length vs decayed: most copies are dead, truncated, point-mutated relics; only a tiny fraction are intact. Solo-LTR : full-length ratio is real biology (recombinational LTR-RT removal rate), measurable only if the assembly resolved full-length elements. Wicker 2007 Nat Rev Genet is the reference scheme; present Gypsy/Copia and the ICTV Metaviridae/Pseudoviridae names both.
Repeat Statistics and Age Landscape with Python
Goal: Summarize masked content by class and plot the Kimura-divergence landscape (a relative within-genome age readout).
Approach: Parse the RepeatMasker .out file, group by class for bp and genome fraction, then histogram percent divergence stratified by major TE class (x = divergence-from-consensus ~ relative age).
import pandas as pd
def parse_repeatmasker_out(out_file):
records = []
with open(out_file) as f:
for i, line in enumerate(f):
if i < 3:
continue
parts = line.split()
if len(parts) < 15:
continue
records.append({'perc_div': float(parts[1]), 'seqid': parts[4],
'repeat_class': parts[10], 'length': int(parts[6]) - int(parts[5]) + 1})
return pd.DataFrame(records)
def repeat_summary(rm_df, genome_size):
by_class = rm_df.groupby('repeat_class')['length'].sum().sort_values(ascending=False)
total = rm_df['length'].sum()
print(f'Total masked: {total/genome_size:.1%} of genome (a LOWER bound; ancient copies decay past detection)')
return by_class / genome_size * 100
The landscape is right-censored - the most ancient TEs decayed past alignment detection, so "no old activity" can mean "old activity is invisible." A sharp left (low-divergence) peak is a recent/ongoing burst; treat presence of a recent peak as informative and absence of an old hump cautiously. A truncated/chimeric consensus distorts the whole x-axis (another reason curation matters); never compare landscapes across genomes annotated with different libraries.
TE Expression from RNA-seq (the Multimapping Minefield)
A read from a young high-copy family maps equally to hundreds of near-identical loci. Unique-only mapping (standard RNA-seq QC) discards most TE signal and biases toward old, uniquely-mappable copies - measuring the least active elements. Use EM/probabilistic reassignment: TEtranscripts/TElocal (Jin 2015), SQuIRE (Yang 2019), Telescope (Bendall 2019). Subfamily-level (TEtranscripts: "L1 went up", high power, no locus) vs locus-level (SQuIRE/TElocal/Telescope: "this HERV-K on chr7 is on", noisy, mappability-sensitive) changes the conclusion, not just the resolution. The dominant false positive: a TE in an intron or downstream of an expressed gene is not "expressed" - read-through/intron-retention piles reads on it; distinguish autonomous transcription from passenger signal by strand and continuity (TEspeX filters embedded-TE reads). Be skeptical of any "TEs reactivated in disease/aging" headline that used unique-only mapping.
Per-Method Failure Modes
Hard-masking before gene prediction
Trigger: running RepeatMasker without -xsmall (default hard-masks with N). Mechanism: masked sequence is destroyed. Symptom: genes overlapping repeats silently absent from the GFF. Fix: -xsmall; hand a soft-masked genome to the predictor.
Host-gene-contaminated library
Trigger: masking with an uncurated de novo library. Mechanism: multicopy gene families look repetitive and enter the library. Symptom: suspiciously few NLR/ZNF/OR genes; domesticated genes (RAG1, CENP-B) missing. Fix: BLAST the library against a protein DB; drop consensi hitting host genes with no TE domain.
Trusting % repeat from a short-read assembly
Trigger: comparing TE content across studies/assemblies. Mechanism: short reads collapse/drop young copies; % depends on library+engine+assembly. Symptom: "low TE, all ancient" or non-comparable cross-study tables. Fix: check LAI/assembly type; report method + assembly with every number; never compare published % across papers.
Discarding multimappers in TE RNA-seq
Trigger: unique-only TE quantification. Mechanism: young high-copy families are not uniquely mappable. Symptom: most TE signal lost, bias to old elements. Fix: EM tools (TEtranscripts/SQuIRE/Telescope); separate read-through from autonomous transcription.
"Unknown" passed off as a result
Trigger: shipping a 40%-Unknown library without inspection. Mechanism: classification is the hardest, last, most-skipped step. Symptom: weak biological annotation; possible gene-family contamination hiding in Unknown. Fix: RepeatClassifier/DeepTE to triage; curate; note DB-coverage limits.
Quantitative Thresholds
| Threshold | Source | Rationale |
|---|
-xsmall soft-mask before gene prediction | predictor requirement | hard-mask truncates repeat-overlapping genes |
| TE content scales with genome size (human ~50%, maize ~85%, Arabidopsis ~20-25%, fungi ~1-20%) | clade norms (approx) | main driver of the C-value enigma; sanity-check vs genome size |
| "Unknown" ~<15% (mammal) vs 30-50% (non-model) | DB coverage | high Unknown bounds biological claims; very low on non-model = over-assignment |
| LAI <10 draft / 10-20 reference / >20 gold | Ou 2018 NAR | LTR-RT-resolution metric; only valid for LTR-rich genomes |
| Report library + engine + assembly with any % | reproducibility | % masked is non-comparable across methods |
| 80-80-80 (≥80% id over ≥80% length over ≥80 bp) | Wicker lineage | dereplication threshold, NOT a quality check |
Common Errors
| Error / symptom | Cause | Solution |
|---|
| Gene prediction finds too few genes | hard-masked, or over-masked low-complexity | -xsmall; -nolow before gene prediction |
| Suspiciously few NLR/ZNF/OR genes | uncurated library masked gene families | decontaminate library against a protein DB |
| Low masking percentage | novel repeats absent from DB | run RepeatModeler2 first; union de novo + Dfam |
| RepeatModeler very slow | normal for large genomes | -threads; consider EDTA (plants) or EarlGrey |
| "TE re-activated" result looks too clean | unique-only mapping / read-through | EM tools; check strand + continuity from neighbor |
| Cross-study % repeat disagree | different library/engine/assembly | re-annotate uniformly; report method |
References
- Flynn JM, et al. 2020. RepeatModeler2 for automated genomic discovery of transposable element families. PNAS 117:9451-9457.
- Storer J, et al. 2021. The Dfam community resource of transposable element families, sequence models, and genome annotations. Mob DNA 12:2.
- Ou S, et al. 2019. Benchmarking transposable element annotation methods for creation of a streamlined, comprehensive pipeline (EDTA). Genome Biol 20:275.
- Ou S, Jiang N. 2018. LTR_retriever: a highly accurate and sensitive program for identification of long terminal repeat retrotransposons. Plant Physiol 176:1410-1422.
- Ou S, Chen J, Jiang N. 2018. Assessing genome assembly quality using the LTR Assembly Index (LAI). Nucleic Acids Res 46:e126.
- Wicker T, et al. 2007. A unified classification system for eukaryotic transposable elements. Nat Rev Genet 8:973-982.
- Baril T, Galbraith J, Hayward A. 2024. Earl Grey: a fully automated user-friendly transposable element annotation and analysis pipeline. Mol Biol Evol 41:msae068.
- Goubert C, et al. 2022. A beginner's guide to manual curation of transposable elements. Mob DNA 13:7.
- Jin Y, et al. 2015. TEtranscripts: a package for including transposable elements in differential expression analysis of RNA-seq datasets. Bioinformatics 31:3593-3599.
- Yang WR, et al. 2019. SQuIRE reveals locus-specific regulation of interspersed repeat expression. Nucleic Acids Res 47:e27.
- Bendall ML, et al. 2019. Telescope: characterization of the retrotranscriptome by accurate estimation of transposable element expression. PLoS Comput Biol 15:e1006453.
- Benson G. 1999. Tandem repeats finder: a program to analyze DNA sequences. Nucleic Acids Res 27:573-580.
Related Skills
- eukaryotic-gene-prediction - Receives the soft-masked genome; over-masking is a shared failure
- annotation-qc - LAI and repeat-content sanity in the assembly-to-annotation handoff
- genome-assembly/assembly-qc - Assembly type sets the TE-annotation ceiling (LAI)
- differential-expression/deseq2-basics - Differential TE expression from TEtranscripts/SQuIRE counts
- copy-number/recurrent-cnv - Segmental duplications, a distinct phenomenon from interspersed repeats
