bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Aug. 6, 2023
Abstract
Background
Many
biological
and
medical
questions
are
answered
based
on
the
analysis
of
sequence
data.
However,
we
can
find
contaminations,
artificial
spike-ins,
overrepresented
rRNA
sequences
in
various
read
collections
assemblies;
complicating
data
making
interpretation
difficult.
In
particular,
spike-ins
used
as
controls,
such
those
known
from
Illumina
(PhiX
phage)
or
Nanopore
(DNA
CS
lambda
phage,
yeast
enolase
ENO2),
often
not
considered
contaminants
also
appropriately
removed
during
bioinformatics
analyses.
Findings
To
address
this,
developed
CLEAN,
a
pipeline
to
remove
unwanted
both
long
short
sequencing
techniques
wide
range
use
cases.
While
focusing
removing
their
technology-specific
control
sequences,
be
for
everyday
tasks,
host
decontamination
metagenomic
reads
assemblies,
removal
RNA-Seq
The
results
purified
identified
contaminated
with
statistics
summarized
an
HTML
report.
Conclusions
decontaminated
output
files
directly
subsequent
analyses,
resulting
faster
computations
improved
results.
Although
is
task
that
seems
mundane,
many
routinely
overlooked,
cleaned
by
steps
fully
reproducible
difficult
trace
user.
CLEAN
will
facilitate
reproducible,
platform-independent
genomics
transcriptomics
freely
available
at
https://github.com/hoelzer/clean
under
BSD3
license.
Proceedings of the Royal Society B Biological Sciences,
Journal Year:
2024,
Volume and Issue:
291(2018)
Published: March 13, 2024
Beneficial
reversals
of
dominance
reduce
the
costs
genetic
trade-offs
and
can
enable
selection
to
maintain
variation
for
fitness.
are
characterized
by
beneficial
allele
a
given
context
(e.g.
habitat,
developmental
stage,
trait
or
sex)
being
dominant
in
that
but
recessive
where
deleterious.
This
dependence
at
least
partially
mitigates
fitness
consequence
heterozygotes
carrying
one
non-beneficial
their
result
balancing
maintains
alternative
alleles.
Dominance
theoretically
plausible
supported
mounting
empirical
evidence.
Here,
we
highlight
importance
as
mechanism
mitigation
conflict
review
theory
evidence
them.
We
identify
some
areas
need
further
research
development
outline
three
methods
could
facilitate
identification
antagonistic
(dominance
ordination,
allele-specific
expression
ATAC-Seq
(assay
transposase-accessible
chromatin
with
sequencing)).
There
is
ample
scope
new
well
reanalysis
existing
data
through
lens
reversals.
A
greater
focus
on
this
topic
will
expand
our
understanding
mechanisms
resolve
whether
they
variation.
Genetics,
Journal Year:
2022,
Volume and Issue:
220(3)
Published: Feb. 10, 2022
Abstract
Single-cell
RNA
sequencing
is
a
powerful
technique
that
continues
to
expand
across
various
biological
applications.
However,
incomplete
3′-UTR
annotations
can
impede
single-cell
analysis
resulting
in
genes
are
partially
or
completely
uncounted.
Performing
with
hinder
the
identification
of
cell
identities
and
gene
expression
patterns
lead
erroneous
inferences.
We
demonstrate
performing
isoform
tandem
rapidly
improve
annotations.
Using
threespine
stickleback
fish
(Gasterosteus
aculeatus),
we
show
models
from
minimal
embryonic
dataset
retained
26.1%
greater
reads
than
Ensembl
alone.
Furthermore,
pooling
our
isoforms
previously
published
adult
bulk
Iso-Seq
stickleback,
merging
annotation
models,
resulted
marginal
improvement
(+0.8%)
over
only
dataset.
In
addition,
identified
by
included
thousands
new
splicing
variants.
The
improved
obtained
using
led
successful
types
increased
many
Our
work
illuminates
as
cost-effective
efficient
mechanism
annotate
genomes
for
sequencing.
Genome Research,
Journal Year:
2024,
Volume and Issue:
34(11), P. 1719 - 1734
Published: Nov. 1, 2024
Long-read
sequencing
(LRS)
technologies
have
the
potential
to
revolutionize
scientific
discoveries
in
RNA
biology
through
comprehensive
identification
and
quantification
of
full-length
mRNA
isoforms.
Despite
great
promise,
challenges
remain
widespread
implementation
LRS
for
RNA-based
applications,
including
concerns
about
low
coverage,
high
error,
robust
computational
pipelines.
Although
much
focus
has
been
placed
on
defining
exon
composition
structure
with
data,
less
careful
characterization
done
ability
assess
terminal
ends
isoforms,
specifically,
transcription
start
end
sites.
Such
is
crucial
completely
delineating
full
molecules
regulatory
consequences.
However,
there
are
substantial
inconsistencies
both
coordinates
reads
spanning
a
gene,
such
that
often
fail
accurately
recapitulate
annotated
or
empirically
derived
molecules.
Here,
we
describe
specific
identifying
quantifying
how
these
issues
influence
biological
interpretations
data.
We
then
review
recent
experimental
advances
designed
alleviate
problems,
ideal
use
cases
each
approach.
Finally,
outline
anticipated
developments
necessary
improvements
from
Peer Community Journal,
Journal Year:
2025,
Volume and Issue:
5
Published: Jan. 13, 2025
Sexual
dimorphism
can
evolve
through
sex-specific
regulation
of
the
same
gene
set.
However,
sex
chromosomes
also
facilitate
this
by
directly
linking
expression
to
sex.
Moreover,
differences
in
content
between
heteromorphic
contribute
sexual
dimorphism.
Understanding
patterns
sex-biased
across
organisms
is
important
for
gaining
insight
into
evolution
and
chromosomes.
studying
species
with
recently
established
help
understand
evolutionary
dynamics
loss
dosage
compensation.
The
three-spined
stickleback
known
its
strong
dimorphism,
especially
during
reproductive
period.
Sex
determined
a
young
XY
chromosome
pair
non-recombining
region
divided
three
strata,
which
have
started
degenerate.
Using
high
multiplexing
capability
3′
QuantSeq
sequence
transcriptome
liver,
gills,
brain,
we
provide
first
characterization
transcriptomes
from
~80
sticklebacks
(40
males
40
females)
collected
natural
population
We
find
that
liver
extremely
differentiated
sexes
(36%
autosomal
genes)
reflects
ongoing
reproduction,
while
brain
shows
very
low
levels
differentiation
(0.78%)
no
functional
enrichment.
Finally,
gills
exhibit
(5%),
suggesting
should
be
considered
physiological
ecotoxicological
studies
gill
responses
fishes.
hemizygous
genes
mainly
driven
lack
conserved
copies
on
both
likely
degeneration
Y
allele
down-regulation
male-beneficial
mutations
X
chromosome.
Genes,
Journal Year:
2025,
Volume and Issue:
16(2), P. 187 - 187
Published: Feb. 3, 2025
Background/Objectives:
Apis
cerana
development
is
described
as
comprising
four
stages:
embryo,
larva,
pupa,
and
adult.
There
are
significant
differences
between
workers
drones
in
terms
of
physiological
functions
social
roles,
the
formation
organ
primordia
occurs
during
embryonic
stage.
Therefore,
objective
this
study
to
investigate
differential
expression
alternative
splicing
genes
worker
drone
embryos
explain
their
unique
developmental
patterns.
Methods:
Long-read
sequencing
(PacBio
Iso-Seq)
short-read
(Illumina
RNA-Seq)
were
used
embryo
gene
A.
across
five
points
(12,
24,
36,
48,
60
h).
Results:
The
identified
59,254
common
isoforms,
with
5744
5106
isoforms
specific
embryos,
respectively.
Additionally,
a
new
transcript
csd
was
identified.
number
differentially
expressed
(3391)
events
(470
genes)
peaked
at
24-h
Differential
csd,
dsx,
Y-y
observed
embryos.
Conclusions:
results
indicated
that
point
critical
period
for
related
behavioral
drones.
findings
provide
theoretical
basis
future
research
on
BMC Biology,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: March 5, 2025
Populations
colonizing
contrasting
environments
are
likely
to
undergo
adaptive
divergence
and
evolve
ecotypes
with
locally
adapted
phenotypes.
While
diverse
molecular
mechanisms
underlying
ecotype
have
been
identified,
less
is
known
about
their
interplay
degree
of
divergence.
Here
we
integrated
epigenomic
transcriptomic
data
explore
the
interactions
among
gene
expression,
alternative
splicing,
DNA
methylation,
microRNA
expression
gauge
extent
which
patterns
at
four
levels
aligned
in
a
case
postglacial
between
marine
freshwater
nine-spined
sticklebacks
(Pungitius
pungitius).
Despite
significant
genome-wide
associations
variation,
found
largely
non-parallel
across
levels,
predominantly
nonoverlapping
(ranging
from
43.40
87.98%)
sets
differentially
expressed,
spliced
methylated
genes,
candidate
genes
targeted
by
expressed
miRNA
ecotypes.
Furthermore,
variation
different
mechanisms,
differential
methylation
splicing
showing
highest
lowest
ecotypes,
respectively.
Finally,
enrichment
associated
methylation.
Our
results
suggest
nuanced
relationship
processes,
alignment
level
masking
relatively
independent
effects
on
level.